• Assist the regulatory team with Institutional Review Board (IRB) preparation and submission, including collation and preparation of documents.
• Screen and schedule participants in a variety of clinical research programs and/or studies.
• Consent subjects and/or families for registry or non-interventional research studies.
• Prepare for and take part in site initiation, monitoring, closeout visits, and document storage activities.
• Conduct and document visits and testing/interviews according to all regulatory and organizational protocols.
• Collect, prepare, process, ship and maintain inventory of research specimens.
• Maintain subject-level documentation and prepare documents, equipment and/or supplies.
• Provide input for and assist with developing IRB-related documents.
• Collaborate with coordinating staff to maintain appropriate documentation.
• Assist in identifying issues related to operational efficiency and share results with supervising coordinator staff and/or management.
• Maintain compliance with institutional requirements and policies.
• Maintain a familiarity with the ethical conduct of research and safeguards needed when conducting clinical research.
• Participate in sponsor-required training.
• Participate in team meetings.
• Proactively includes others in decision-making and escalates issues to management.
• Investigate incomplete, inaccurate, or missing data/documents to ensure accuracy and completeness of data.
• Recognize and report vulnerabilities related to the security of physical and electronic data.
• Adhere to and participate in the development and assessment of quality assurance.
• Assist with recognizing trends related to data quality and escalation.
• Utilize electronic data capture systems, technologies and software necessary for clinical research program and/or study operations.
• Score tests, enter data and complete required forms accurately and according to protocol.
• Assist with the development of data collection documents and instruments.
• Identify issues related to data capture, collection, or management and escalate to supervising coordinator staff and/or management.
• Ensure participant care expenses have appropriate financial routing and subjects are paid as relevant for participation in clinical trials.

Skills: IRB Submissions, Participant Screening, Informed Consent, Regulatory Compliance, Clinical Documentation, Specimen Management, Data Entry, Quality Assurance

• Coordinate the implementation, both internally and externally, of a sponsored clinical research study, including conducting approaches, consents and randomization of participants.
• Work in concert with the Principal Investigator and/or Research Manager, develop and implement patient recruitment strategies.
• Recruit and evaluate potential study patients.
• Oversee baseline questionnaires per protocol instructions and coordinate with research therapists to assign intervention patients.
• Maintain contact with study participants and coordinate study visits.
• Answer any phone calls and inquiries regarding the study protocol.
• Refer participants to the supervisor or clinical staff.
• Send a 6-week questionnaire and track responses, or administer the questionnaire by phone.
• Responsible for the coordination and implementation of infant and childhood follow-up of study participants, including coordination with multidisciplinary staff.
• Develop, organize, and/or maintain detailed clinical and research databases.
• Use programs such as Excel and REDCap.
• Responsible for data validation and quality control.
• Manage communication and logistics for all study stakeholders, including participants and the IRB.

Skills: Clinical Study Coordination, Participant Recruitment, Informed Consent, Patient Follow-Up, Questionnaire Administration, Data Management, REDCap Proficiency, Stakeholder Communication

• Write and create assessments utilizing standard research protocol.
• Assist in grant proposal writing.
• Assist in communications with researchers and members of the research community.
• Arrange and conduct experiments for a research study, including explaining the goals of the study and arranging for the evaluation.
• Follow up by phone, email, and email with research colleagues.
• Participate in the preparation and delivery of presentations to disseminate study findings.
• Analyze data and draft data reports, manuscripts, and presentations.
• Utilize approved procedures.
• Administer involved, systematic tests, including the assessment and/or response.
• Help maintain study procedure documentation.
• Prepare study-related materials.
• Assist with data entry, cleaning, and guided analysis.
• Monitor experiments as required by the study protocol.
• Utilize study-related devices and equipment as part of assessment procedures.
• Maintain study records and edits for completeness and accuracy.
• Attend regular team meetings.
• Troubleshoot field issues.
• Use discretion to resolve issues when unplanned events arise.

Skills: Research Assessments, Grant Writing Support, Research Communication, Experimental Coordination, Data Analysis, Scientific Reporting, Study Documentation, Protocol Compliance

• Call potential study participants to tell them more about the outreach initiative.
• Interview caregivers of young children using the provided questionnaires.
• Abstract data and data entry to medical charts.
• Enter data from interviews and chart review into the data collection computer program.
• Conform to hospital standards of performance and conduct, including those pertaining to patient rights, so that the best possible customer service and patient care may be provided.
• Utilize the hospital's behavioral standards as the basis for decision-making and to facilitate the hospital's goals and mission.
• Follow established hospital infection control and safety procedures.
• Adhere to all of BMC's RESPECT behavioral standards.

Skills: Participant Outreach, Caregiver Interviewing, Data Abstraction, Data Entry, Patient Rights, Hospital Compliance, Infection Control, Professional Conduct

• Provide administrative support with protocol distribution at research clinics.
• Support the research nurse in locating the patient’s research chart for patient visits and data collection.
• Prepare research charts for upcoming visits by ensuring current source documents are on the chart, correct labs are ordered, and a new version of the ICF is printed.
• Responsible for taking phone messages.
• Collect data from existing records for real-time data collection.
• Provide the research nurse with assistance in ensuring research documents are completed in a timely manner.
• File documents in the research chart.
• Ensure there is an adequate stock of office supplies and equipment for all research clinics.
• Schedule and coordinate meetings, appointments and calendars for research nurses.
• Track and assist in obtaining outstanding training for nurses and investigators.
• Track patients’ reconsent documents.
• Assist in prioritizing queries based on due date and importance.
• Facilitate in obtaining of signatures on necessary documents, including but not limited to AE and RECIST logs.
• Updates lab kit request logs for all clinics on a weekly basis.
• Fax and scan documents to the appropriate departments.
• Send study correspondence to the appropriate persons.

Skills: Research Administration, Chart Preparation, Clinical Documentation, Data Collection, Scheduling Coordination, Training Tracking, Document Filing, Office Management

• Use knowledge of qualitative methods to help develop focus group guides/interview scripts.
• Assist/India team with adapting the TFT-TFS program to Madhya Pradesh, developing smartphone training and data collection, and writing study protocols.
• Assist with the development of process and cost tracking systems.
• Maintain communications (meetings, email, phone) between the and Indian-based investigators and staff.
• Assist with the coordination and preparation of project-related meetings, including taking meeting minutes.
• Prepare and submit study protocols, project materials, and amendments to the Institutional Review Board (IRB), annual reports to the National Institutes (NIH), and other reports.
• Maintain and update the study timeline and documentation.
• Assist with logistical needs of the study, such as processing honoraria, arranging travel, food service, and conference room scheduling.
• Assist investigators with data analysis and manuscript preparation.
• Conduct relevant literature searches and reviews.

Skills: Qualitative Methods, Focus Group Guides, IRB Submissions, International Coordination, Project Documentation, Meeting Coordination, Data Analysis, Literature Review

• Use standard operating procedures, implement a system (developed by the project director) for screening, recruiting, and testing Veteran participants in research and program development settings.
• Devise and recommend alternative methods of data collection and help to implement new methods.
• Coordinate and conduct project-based interaction with Veteran participants, developing a system for tracing project positions, and monitoring the project processes, including recruitment, screening, progress through the program, and evaluation of outcomes.
• Prepare reports detailing the progress of data collection efforts.
• Evaluate and implement project protocols for assessing participants.
• Administer questionnaires, cognitive and assessment tools, including structured interviews as well as tests of cognition, memory, attention, and executive function.
• Screen study participants and follow procedures that track study progress.

Skills: Participant Screening, Veteran Recruitment, Data Collection, Protocol Implementation, Questionnaire Administration, Cognitive Testing, Progress Reporting, Study Coordination

• Order and organize supplies and research reagents.
• Maintain mouse colonies, breeding, and genotyping.
• Maintain lab equipment and oversee compliance with Biosafety guidelines.
• Assist with animal surgeries.
• Assist in performing tissue sectioning and staining, imaging, cell culture and molecular biology experiments.
• Contribute directly to research projects or be assigned.

Skills: Supply Management, Animal Care, Genotyping, Biosafety Compliance, Surgical Assistance, Tissue Processing, Cell Culture, Molecular Biology

• Isolate and perform quality control of DNA and RNA from environmental samples.
• Extract high-quality genomic DNA for next-generation sequencing.
• Troubleshoot and optimize existing protocols.
• Assist with outdoor and indoor field sampling.
• Handle and maintain cultures of microbial isolates.

Skills: DNA RNA Isolation, Genomic DNA Extraction, Quality Control, Protocol Optimization, Field Sampling, Environmental Sampling, Microbial Culturing, Culture Maintenance

• Conduct document analysis of government website and social media accounts.
• Write up research findings in briefs for the project team and other project outputs.
• Participate in interviews with policymakers and inthe analysis of the interview data.
• Respond to project-related emails.
• Attend project meetings.
• Prepare progress reports for investigators and the funding agency.

Skills: Policy Analysis, Research Briefs, Interview Analysis, Stakeholder Communication, Email Management, Meeting Participation, Progress Reporting, Policy Research

• Conduct interview assessments with research participants using psychiatric rating scales and other validated questionnaires.
• Perform data collection for the study.
• Monitor the implementation of risk assessment procedures for each trial participant, ensuring that participant care is appropriate to the perceived risk while maintaining the patient’s dignity and rights.
• Demonstrate a commitment to actively managing the environmental risks encountered.
• Coordinate invitations and appointments for study participants, including recruiting new participants, conducting trial interviews.
• Follow up of missed appointments, obtaining address details and necessary consent forms from study participants, conducting assessments and interviews and collecting other relevant data, and data entry.
• Manage the research project on a day-to-day basis by ensuring that data is being collected and stored appropriately according to the procedural requirements of the research project and conforming to good clinical practice guidelines.
• Communicate and liaise with other research staff within IMPACT and Barwon Health, and other trial collaborating groups.
• Apply experience with the principles of good clinical practice and a commitment to operate within these guidelines.
• Maintain strict standards of confidentiality.
• Attend relevant meetings and participate in the planning and review of the trial research protocol and related activities.
• Participate in Quality Assurance procedures related to the project and service, including any necessary training and review meetings implemented across trial sites.
• Cooperate with all health and safety policies and procedures of the university and take all reasonable care to ensure that actions or omissions do not impact the health and safety of yourself or others.

Skills: Clinical Interviews, Psychiatric Assessments, Risk Monitoring, Participant Scheduling, Data Collection, Good Clinical Practice, Research Coordination, Quality Assurance

• Perform a variety of routine laboratory experiments and procedures according to prescribed protocols and assigned schedules, utilizing standard laboratory equipment and recording and checking results for completeness and accuracy.
• Assist in troubleshooting procedures if experimental results are unexpected or the quality of specimens is poor.
• Maintain records of results and methodologies in a log of work performed.
• Maintain equipment, lab area and supplies in a neat, professional manner.
• Sterilize and clean glassware, prepare media and other materials using appropriate procedures.
• Inventory supplies alert the supervisor to needed supplies or mixes standard reagents.
• Process order for supplies and/or animals.
• Attend courses in safety procedures for handling, storage and disposal of biohazardous, flammable, corrosive and toxic materials.
• Carry out all laboratory activities in compliance with applicable regulations and protocols.
• Conduct literature searches and reviews, compiling information for journals and suggesting uses for new techniques to the P.I.
• Attend courses, lectures and conferences to further one's knowledge of research and laboratory techniques, consulting with other researchers and technicians to exchange information.
• Contribute to the team within and between departments and organizations.

Skills: Laboratory Techniques, Protocol Compliance, Experimental Troubleshooting, Data Recording, Equipment Maintenance, Reagent Preparation, Safety Compliance, Literature Review

• Execute experimental studies in support of lab goals and grant commitments, studying human immune responses to viral vaccines.
• Assist in the planning, design and modifications of experiments.
• Prepare tables/charts/graphs and assist in organizing data.
• Make presentations in laboratory meetings and may contribute to the writing of manuscripts.
• Maintain lab equipment and supplies.
• Process and ship samples, isolate PBMC, DNA, and RNA, perform antibody and cytokine ELISA, ELISPOT, flow cytometry, and cell culture, and grow various viruses.

Skills: Immunology Experiments, Experimental Design, Data Visualization, Scientific Presentations, Manuscript Support, Sample Processing, Flow Cytometry, Cell Culture

• Responsible for data entry (transferring data from paper formats into electronic databases, such as Excel).
• Create and update forms on various online platforms (e.g., SurveyMonkey, Qualtrics).
• Accountable for data collection activities.
• Prepare data collection documents.
• Create and maintain spreadsheets to track incoming data and data collection progress from multiple data collectors nationwide.
• Regularly communicating and troubleshooting with and answering questions for data collectors.
• Accountable for basic data processing and quality checks.
• Responsible for exporting and cleaning data.
• Responsible for summary report writing.
• Produce narrative and basic descriptive analyses to summarize customer learning experiences.
• Responsible for manuscript preparation.
• Apply knowledge of APA style formatting.

Skills: Data Entry, Online Forms, Data Collection, Spreadsheet Tracking, Data Cleaning, Quality Checks, Report Writing, APA Formatting

• Assist the Coordinator and/or Investigator with managing the routine, day-to-day activities of the program, including conducting structured interviews, collecting data, and maintaining records, documents, and data.
• Collect and ship specimens, per study protocol specifications.
• Complete and maintain all program-related records for each participant, including consent forms, data management system, and source documentation worksheets.
• Develop appropriate processes for updating and maintaining records.
• Independently responds to general inquiries from program participants, staff and other stakeholders.
• Independently drafts correspondence and general communications regarding the program, including memorandums and reports as requested by the PI.
• Assist with scheduling meetings, including arranging for space, notifying participants, preparing the agenda and minutes and following up on all commitments to ensure that necessary arrangements have been made.
• Prepare documents and research matters for the staff, including documents of a confidential and/or technical nature.
• Organize the information, develop reports, and highlight the most important portions for the staff.
• Responsible for inputting data into several electronic databases, which might include Microsoft Outlook, Excel, Word, PowerPoint, Access, LIMBS, IFCAO, and other databases.
• Extract data to prepare reports, sort and summarize data elements, and manipulate data by performing statistical queries that are pre-programmed or built within Microsoft or VA software.
• Relieve the coordinator of administrative details based on knowledge of program responsibility and the management requirements of the supervisor.
• Plan and perform other related administrative follow-up duties independently and on own initiative.
• Coordinate policies as well as monitor and control reports.
• Maintain the research laboratory facilities, equipment and control supplies.
• Maintain such equipment as centrifuges, refrigerators, freezers, spectrophotometers, PCR machines, western blotting machines, biosafety hoods, and analytical balances.
• Monitor research specimens, equipment, and the environment.
• Assist in the purchase, inventory, and distribution of various research laboratory supplies or commercial media.
• Obtain pricing quotes for purchases through communication with vendor personnel.
• Process requisitions, receive, and store shipments, noting damage, contamination, shortage or other errors in shipment.
• Reconcile shipments with original orders, and package products for pick up or shipment.
• Follow safety guidelines for required research procedures and equipment operation.
• Work with other labs, the research administration, and other departments to solve common and uncommon issues that arise in a timely manner.
• Manage implementation, control and reporting on clinical tests.
• Maintain records and prepare project administrative and statistical reports.
• Draft and maintain all documentation required for the clinical portion of participation.
• Perform routine clinical tests and studies, including drawing blood, monitoring vital signs, and measuring lung function, body composition and grip strength.

Skills: Program Coordination, Structured Interviews, Specimen Handling, Clinical Data Management, Administrative Reporting, Database Management, Laboratory Operations, Clinical Testing

• Observe and run usability testing sessions, taking notes, as well as providing detailed transcripts for the team.
• Assist with user testing preparation activities, including team collaboration/planning.
• Responsible for coding user research videos.
• Create highlight videos/screenshots, and assist with data analysis and report documentation.
• Assist with overall study and data collection activities.
• Conduct literature reviews.
• Responsible for running competitive analyses.
• Design, run and interpret complex quantitative user studies.
• Prepare user testing activities (ex., create screener, recruit participants, lab setup, coordinate support materials, coordinate studies across multiple teams and stakeholders, etc.)
• Running user research sessions in the lab and field.
• Convey findings and formulate recommendations clearly, utilizing critical thinking.
• Establish rapport with stakeholders, understand their requests and present research findings that address their questions.
• Collaborate with other researchers on reviewing study plans, suggesting methodologies, and assisting with data analysis.

Skills: Usability Testing, User Research, Video Coding, Data Analysis, Literature Review, Competitive Analysis, Quantitative Studies, Stakeholder Communication

• Conduct research in the special collections and contribute to the conceptual development of a project by organizing/creating documentation of found materials, such as bibliographies, searching for and ordering texts, writing literature reviews, etc.
• Request images for exhibitions and/or publications, research and obtain art and image permissions.
• Proofread, edit, and translate.
• Assist with the creation of project websites and PowerPoint presentations.
• Copyedit essays, author biographies, endnotes, etc.
• Assist with organizing art programs for publications by communicating with authors, updating essay drafts, assisting editors in checking page proofs, proofing indexes, etc.

Skills: Archival Research, Literature Reviews, Image Permissions, Proofreading Editing, Translation Support, Website Support, Presentation Design, Publication Coordination

• Assist with subject recruitment, including placing advertisements, phone screening prospective participants, working with the team to schedule research subjects, and collecting clinical and demographic data.
• Schedule and organize visits for all study procedures, blood collection, screening procedures, video visits, phone visits, and interviews.
• Guide participants in proper use of at-home data collection devices (EEG, Actigraphy, and Apnealink) and operating all relevant software in collaboration with the Sleep Data Coordinator.
• Perform data entry, downloading, scanning, and verification.
• Assist with the purchase of study supplies.
• Maintain and update databases, subject information folders, and subject payment forms.

Skills: Subject Recruitment, Participant Scheduling, Clinical Data Collection, Device Instruction, Data Entry, Data Verification, Database Maintenance, Study Logistics

• Provide broad support to support the analysis and dissemination of the Transgender and Gender Diverse Health Equity Study.
• Conduct community engagement initiatives upon request.
• Develop and manage study databases.
• Develop thematic codes and code books for qualitative analysis of in-depth interviews, apply thematic coding schemes to data, attend coding consensus meetings, and summarize themes and findings.
• Conduct literature searches and reviews.
• Prepare data, manuscripts, conference presentations, and other reports.
• Conduct data analysis and interpretation.

Skills: Health Equity Research, Community Engagement, Database Management, Qualitative Coding, Thematic Analysis, Literature Review, Data Analysis, Manuscript Preparation

• Participate in data collection for research projects.
• Prepare data analysis tables and figures, and charts necessary for professional data display.
• Coordinate day-to-day activities of the project to ensure all goals are met.
• Conduct research literature searches for staff and assigned leads.
• Provide one-to-one consultation for staff needing assistance with research literature searches.
• Maintain data files for projects coordinated by the department.
• Coordinate annual report for the department, working closely with the Director on format.
• Assist with professional presentation development department and assigned leads.
• Serve as a resource for PowerPoint, Excel, and other databases.

Skills: Data Collection, Data Visualization, Project Coordination, Literature Searching, Research Consultation, Data File Management, Report Coordination, Presentation Support

• Serve as community advisors for projects with aims focused on young Black gay men residing in the Atlanta area.
• Attend regular meetings(to include some evenings and weekends).
• Actively participate in the development and implementation of recruitment strategies.
• Work with staff to learn fundamental research practices.
• Assist with data collection (i.e., administering surveys, facilitating focus groups, conducting qualitative interviewing, etc.)
• Create innovative ways to disseminate findings back to the community.
• Work with Community Advisors to develop strategies to reach the key population.
• Help keep social media current to reflect pivotal moments taking place now.

Skills: Community Engagement, Recruitment Strategies, Research Practices, Survey Administration, Focus Group Facilitation, Qualitative Interviewing, Findings Dissemination, Social Media Outreach

• Organize laboratory tasks involving team members and collaborators and carry out the experiment.
• Consolidate results and proactively communicate and share them with the project leaders.
• Own experimental expertise and methods and assist colleagues in implementation and use.
• Develop, propose new methodologies and applications, and strengthen and renovate existing methods/methodologies.
• Coordinate experiments for multiple projects in parallel.
• Deliver project objectives according to the project plan.

Skills: Experimental Coordination, Method Development, Technical Expertise, Team Collaboration, Results Reporting, Multi-Project Management, Method Optimization, Project Delivery

• Provide support to Study Directors or other Study Coordinators.
• Initiate, submit and update scheduling requests.
• Draft the initial study protocol and submit to the Study Director.
• Verify accuracy and approve animal orders.
• Establish reporting timelines.
• Coordinate study needs with operational areas independently.
• Coordinate reporting needs with the Study Director.
• Maintain proficiency in basic computer programs and specific software used in study conduct.
• Maintain familiarity with routine study procedures.
• Monitor phases of a study and report issues to the Study Director.
• Manage test article acquisition, MSDS distribution and test article disposition.
• Review data packages from the lab areas and ensure QC findings were completed.
• Prepare the methods section of a report, basic tables, and graphs for the report.
• Review the live phase and contributor reports to assure completeness and accuracy.
• Help ensure reporting timelines are met and draft/final reports are issued to the Sponsor.

Skills: Study Coordination, Protocol Drafting, Scheduling Management, Animal Order Review, Report Preparation, Quality Control Review, Timeline Tracking, Sponsor Reporting

• Maintain and store cell lines under sterile and healthy conditions.
• Follow the ATCC guidelines for cell culture and cryogenic storage.
• Know how to perform oral gavages, IP injection, and measure tumor size.
• Complete training and certification by the Department of Veterinary Medicine to handle and work with live animals, primarily mice, in a safe and humane manner, following institutional guidelines for disposal of dead animals, biohazard and used needles.
• Responsible for ordering laboratory animals and maintaining up-to-date animal inventory.
• Perform cell proliferation (cytotoxicity) assay, soft agar assay, 3D assay, migration, invasion, mammosphere assay, immunohistochemistry staining, immunofluorescence staining, FACS analysis, and western blot.
• Record keeping and maintenance of the Laboratory.
• Responsible for ordering laboratory supplies, maintaining inventory of antibodies, cell lines, plasmids, and preparing common reagents such as buffers and plasmids.
• Participate and help other lab members to promote ongoing projects in the laboratory.
• Keep accurate records of experimental design and results, perform accurate data analysis of experimental results and communicate these records to Pl and other members of the laboratory.
• Compile analyzed research data and submit results to Pl for inclusion in publications, grants or protocols.
• Use knowledge of word processing, spreadsheet software, graphic and statistical programs to create charts, posters and reports of the results.
• Present findings of research projects to laboratory members during laboratory meetings.
• Train visiting scientists and other research staff and students in research procedures and the use of laboratory equipment.
• Demonstrate diligence and willingness to learn and help others in the implementation of new techniques.
• Perform routine maintenance of ultra-low freezers, liquid nitrogen, C02 and water levels.
• Comply with all institutional safety policies, including Universal Precautions and OSHA standards, when handling toxic, hazardous, flammable, radioactive, or potentially infectious or carcinogenic materials.

Skills: Cell Culture, Animal Handling, In Vivo Techniques, Molecular Assays, Immunostaining Methods, Data Analysis, Laboratory Management, Safety Compliance

• Perform data entry and maintain records, reports, and files.
• Obtain the necessary knowledge and skills needed to maintain competency and certifications.
• Maintain patient confidentiality and privacy in accordance with hospital policy.
• Follow experimental protocol and instructions precisely.
• Assist with the entry of patient visits into the clinical trials management system for invoicing.
• Assist with receiving and initial processing of biospecimens.
• Grasp methodologies, techniques, and concepts.
• Work effectively with many people at various levels of the organization.

Skills: Data Entry, Record Management, Patient Confidentiality, Protocol Adherence, Clinical Trial Systems, Biospecimen Processing, Technical Knowledge, Team Collaboration

• Recruit patients to participate in quality improvement studies.
• Conduct patient surveys in person and by phone.
• Responsible for database management.
• Work with study coordinators to provide updates and insights relevant to the research.
• Help manage day-to-day study operations.
• Assist with other aspects of MTQIP/MHEAL operations.
• Conform to Michigan Medicine standards of conduct and performance.

Skills: Patient Recruitment, Survey Administration, Database Management, Research Coordination, Study Operations, Quality Improvement, Data Reporting, Professional Standards

• Assist the Research Consultant with a variety of life and health insurance research matters.
• Perform analysis by applying appropriate protocols in analyzing data and reaching accurate conclusions.
• Write or draft technical reports or related material based on research, investigation, or analysis.
• Analyze, summarize, and/or review data.
• Responsible for interpreting results.
• Responsible for reporting findings.
• Design or use questionnaires, surveys, or other instruments used in the collection and analysis of data.
• Perform research activities by utilizing computer software to obtain and manipulate data.
• Review and evaluate reports, documents, laws, rules, and regulations.
• Answer technical questions regarding data, trends, or results from studies.
• Use computer programs to generate and analyze data.

Skills: Insurance Research, Data Analysis, Technical Reporting, Results Interpretation, Data Summarization, Survey Design, Statistical Software, Regulatory Review

• Assist in developing and preparing project grant proposals, primarily for federal and other unique funding sources, and obtaining support for new and/or continued research activities.
• Perform literature searches.
• Assist the PI with the preparation of academic and research publications.
• Assist with editing and submission of journal articles, as well as writing and editing articles for other publications.
• Advise and assist the PI in planning and preparing presentations of research findings.
• Prepare charts, graphs, tables, and PowerPoint presentations for the PI.
• Assist the PI with writing, submitting, and maintaining regulatory requirements (IRB).

Skills: Grant Proposal Support, Literature Searching, Manuscript Preparation, Journal Editing, Research Presentations, Data Visualization, PowerPoint Development, IRB Compliance

• Gather information from publicly accessible data sources about high net worth individuals, companies and grant-making trusts.
• Responsible for updating the database (Raisers Edge).
• Assist with data analysis.
• Assist with the database screening programme, which may include using screening tools and preparing reports identifying major donor prospects.
• Compile clear and concise briefings and prospect reports for a varied range of clients in the charity sector.
• Report on individuals, grant-making trusts and corporates as well as competitor research.
• Provide support/data entry to the research team.
• Assist with responding to enquiries from current and prospective clients by telephone and email.

Skills: Prospect Research, Database Updating, Data Analysis, Donor Screening, Report Writing, Competitive Research, Data Entry, Client Communication

• Collect and log experimental data.
• Keep a record of information obtained during the research, including a database of information, hard files, etc.
• Ensure compliance with the protocol, ISO, and overall objectives.
• Conduct statistical analyses of data sets.
• Maintain laboratory equipment and inventory.
• Conduct and oversight clinical data collection in health facilities.
• Review literature to gather information.

Skills: Data Collection, Data Logging, Protocol Compliance, Statistical Analysis, Equipment Maintenance, Clinical Data Collection, Literature Review, Inventory Management

• Develop, implement, and evaluate marketing strategies for CE communications using a variety of efforts such as CE impact stories.
• Host dissemination consultations with community-academic partners.
• Manage CE Bridges, CE’s monthly e-newsletter.
• Collaborate with MICHR Communications to promote CE efforts among MICHR, Michigan Medicine, U-M, peer-reviewed journals, and mainstream media channels.
• Support planning and administering CE’s annual Building Bridges, Breaking Barriers in Translational Research Retreat, and other CE events, including town halls, CE Studios, funding webinars, pop-up networking gatherings, and conference sessions.
• Actively engages in and supports partnership development efforts across communities and U-M schools and departments.
• Serve as program coordinator for an online hub for community engagement in research.
• Facilitate fresh content for M-REACH, which includes uploading resources to help community-academic partners stay abreast of emerging information in the field of CEnR, building capacity for CEnR, and providing training opportunities.
• Staff a Network Advisory Committee (NAC) of community-academic partners charged with providing leadership and recommendations to enhance the M-REACH hub.
• Review and reflect on information describing the platform’s metrics/performance, user satisfaction, as well as suggest strategies to recruit users, and identify hub enhancements.
• Staff and facilitate NAC meetings, prepare agendas and preparatory materials, and complete all follow-up tasks such as meeting minutes.
• Work with MICHR’s Design and Innovation Core on M-REACH hub enhancements.
• Remain amenable to training to upload documents, run reports, and perform other duties.
• Support the development and execution of M-REACH products and services.
• Support planning a staff-faculty retreat to review metrics and outcomes from the 5-year funding period, and to begin to operationalize the next 5-year funding period.

Skills: Community Engagement Marketing, Strategic Communications, Newsletter Management, Partnership Development, Event Coordination, Program Coordination, Content Management, Performance Analysis

• Assist with the development and implementation of communication plans, engaging with stakeholders on a regular basis to promote the objectives of the RSC-ERGs and facilitating the successful Conduct of the research projects.
• Responsible for data collection, storage and preliminary analysis of data collected in accordance with research protocols and requirements.
• Contribute to the drafting of reports, scholarly papers, and conference presentations.
• Coordinate meetings and activities between researchers and participating external collaborators.
• Assist in the analysis and interpretation of data from the research projects, and their presentation to a diverse audience, including RACGP staff, academics, clinicians, educators, and government agencies.

Skills: Stakeholder Engagement, Communication Planning, Data Collection, Data Analysis, Research Reporting, Meeting Coordination, Data Interpretation, Research Presentation

• Screen and consent patients for research studies in the clinic.
• Administer Health-Related Quality of Life surveys to patients in the clinic.
• Review patient charts to gather radiographic, operative, and clinical data.
• Gather references and images to edit and format research papers.
• Draft IRB (Institutional Review Board) documentation for research studies.
• Support physicians in tasks associated with project development, implementation, data collection, data analysis, manuscript preparation, and presentation.
• Manage databases, including data exportation and manipulation, as well as online surveys and database development.

Skills: Patient Screening, Informed Consent, Survey Administration, Chart Review, IRB Documentation, Research Support, Database Management, Manuscript Preparation

• Complete all training for precise delivery of study subject assessments (including but not limited to neuropsychological battery, CAM ICU 7, geriatric depression scale, and physical assessments).
• Review electronic medical records to determine eligibility of patient for study.
• Work with hospital staff to determine LAR for the subject.
• Assist the Research Coordinator in developing advertising and other recruitment tools.
• Recruit patients, marketing the benefits of the study, obtaining informed consent, completing all necessary documentation, and conducting final screening.
• Provide education to the patient regarding trial participation, including information regarding incentives.
• Deliver study intervention utilizing iPad and wireless headphones.
• Document subject feedback, critically assess, and present potential solutions to the study team.
• Complete electronic entry of study data in a timely and accurate manner and participate in quality audits.
• Securely maintains study files in an organized manner and assists new staff in doing the same.
• Ensure the availability of supplies and equipment and initiate purchases to meet the needs of the study.
• Participate and provide input to study quality improvement and progress meetings to continuously improve study processes, efficiency, security and compliance.
• Transport bio-specimen samples to laboratory storage facilities and maintain accompanying documentation.

Skills: Patient Screening, Informed Consent, Clinical Assessments, Participant Recruitment, Study Interventions, Data Entry, Quality Audits, Specimen Transport

• Collect and study primary human tissue under direct supervision.
• Perform PCR, qRT-PCR, and NGS under direct supervision.
• Read and follow all experimental protocols and accurately document all laboratory activities.
• Order laboratory reagents and maintain laboratory equipment.
• Maintain chemical and biological inventory.
• Maintain safety documentation.
• Relate data to the PI in written, graphical and oral communications.

Skills: Human Tissue Handling, PCR Techniques, NGS Support, Protocol Compliance, Laboratory Documentation, Reagent Ordering, Inventory Management, Scientific Communication

• Under moderate supervision, conduct and evaluate experiments and assays.
• Understand and follow experimental protocols (may include animal handling, tissue culture, etc.)
• Record, compile, interpret, and communicate data/results.
• Follow University safety protocols (may include use of combustibles, radioactivity, toxic material, and/or carcinogens).
• Perform calculations involving molarity, % solutions, and serial dilutions.
• Prepare, operate and troubleshoot equipment in experimental procedures.
• Read and follow all equipment manuals.
• Maintain and repair equipment according to manufacturer and University guidelines.
• Ensure the Laboratory is prepared for experiments.
• Accountable for maintaining inventories.
• Maintain sterile conditions.
• Responsible for preparing reagents.
• Demonstrate an understanding of acceptable procedures and techniques.
• Recognize problems and suggest solutions.
• Assist in modifications.
• Provide appropriate written documentation of experiments.
• Prepare preliminary research progress reports.
• Summarize test results appropriately.

Skills: Experimental Assays, Protocol Adherence, Data Interpretation, Laboratory Safety, Solution Preparation, Equipment Operation, Inventory Management, Technical Documentation

• Perform assays and research procedures according to the lab standard operating procedures (SOPs).
• Record experimental techniques and data according to laboratory protocol.
• Calculate accurate test results for statistical purposes.
• Maintain laboratory and equipment according to SOPs.
• Document and report problems to appropriate personnel.
• Fulfill continuing education and regulatory requirements related to research performed, including safety and compliance training.

Skills: Laboratory Assays, SOP Compliance, Data Recording, Statistical Calculations, Equipment Maintenance, Problem Reporting, Regulatory Compliance, Safety Training

• Perform computer programming and experiments as instructed by the Principal Investigator (PI).
• Gather, organize, and record data.
• Perform a simple analysis of results.
• Assist with library and/or electronic research.
• Incorporate new protocols and methodology into work as directed by PI and/or senior lab staff.
• Attend weekly journal clubs, department seminars and lab meetings.
• Present research results at national and local meetings.
• Assist in ordering supplies.
• Maintain orderly records of purchases.

Skills: Computer Programming, Data Collection, Data Analysis, Literature Research, Protocol Implementation, Research Presentation, Supply Ordering, Record Keeping

• Provide assistance on clinical research studies as per study guidelines and protocols.
• Conduct telephone interviews or schedule patients for study visits and screenings per protocol instructions.
• Perform clinical tests such as phlebotomy, EKGs, etc.
• Interact with patients/subjects with regard to the study, including patient education, procedural instruction, and follow-up.
• Serve as a liaison between the patient and the physician.
• Responsible for collecting data and maintaining the patient information database for the study.
• Input data, perform minimal analysis, and run various reports.
• Maintain patients' records as part of record record-keeping function.
• Responsible for mailing various study information or packets to study participants.
• Monitor and set up equipment.
• Maintain inventory and order supplies.

Skills: Clinical Research Support, Patient Scheduling, Clinical Testing, Patient Education, Physician Liaison, Data Management, Record Keeping, Equipment Setup

• Assist PI, research staff, and students with various lab procedures and projects.
• Apply common sense understanding to carry out instructions furnished in written, oral, or diagram form.
• Deal with problems involving several concrete variables in standardized situations.
• Perform experiments as instructed by the Principal Investigator and perform the techniques required in experiments.
• Perform basic lab tasks required to complete experiments.
• Prepare reagent solutions, buffers and media.
• Monitor inventory of essential lab supplies and order additional supplies.
• Help maintain a safe and orderly lab environment.
• Ensure compliance with safety regulations.

Skills: Laboratory Assistance, Experimental Techniques, Reagent Preparation, Protocol Adherence, Problem Solving, Inventory Monitoring, Lab Organization, Safety Compliance

• Run experiments, assays, and record results.
• Compile and communicate results to the supervisor.
• Prepare and operate equipment in experimental procedures.
• Operate equipment such as a blood gas analyzer, centrifuge, pH meter, spectrophotometer, autoclave, scintillation counter, electrophoresis unit, analytical balance, etc.
• Responsible for cleaning equipment.

Skills: Experimental Assays, Data Recording, Results Reporting, Equipment Operation, Laboratory Instrumentation, Sample Processing, Equipment Cleaning, Lab Maintenance

• Perform administrative duties including scheduling, coordinating sites, managing projects, liaising with partners, collaborators, and other McLean staff, and preparing documents for broad dissemination.
• Accountable for data analysis activities, including statistical programming in R to process large datasets of cognitive test data.
• Research support activities include work with local Institutional Review Boards, coordinating and running research studies, participant/patient recruitment, managing and analyzing research data, preparing grants and manuscripts for publication, as well as literature reviews.
• Attend weekly laboratory meetings.
• Monitor patients’ participation in studies while providing regular updates regarding their progress.
• Collaborate with lab members in the development of technical and research skills.
• Develop scientific software to build custom studies and questionnaires and refine cognitive tests.
• Support of the BaCH Tech Lab and Dr. Singh’s ongoing studies.

Skills: Administrative Coordination, Project Management, Statistical Programming, Research Data Analysis, IRB Coordination, Participant Monitoring, Scientific Software, Manuscript Preparation

• Assist the Principal Investigator (PI), research staff, and students with various lab procedures and projects.
• Perform straightforward lab assays as instructed by the PI.
• Collect and organize data, perform data entry and analysis, and conduct literature searches.
• Incorporate new information/techniques into experiments with PI’s approval.
• Maintain professional records of experiments conducted.
• Communicate transparently with the PI about any difficulties and/or errors so that solutions can be implemented.
• Prepare solutions, buffers and media.
• Adhere to safety regulations and university policies.

Skills: Laboratory Assistance, Basic Assays, Data Collection, Data Analysis, Literature Search, Experimental Documentation, Reagent Preparation, Safety Compliance

• Monitor and maintain the health and welfare of the lab’s butterfly colonies and milkweed lines at all sites (Biological Sciences Building, Matthaei Botanical Gardens).
• Develop and maintain a robust pest management plan and keep detailed records.
• Manage appropriate permits.
• Adhere to all University of Michigan policies and procedures for laboratory/greenhouse research.
• Maintain databases of butterfly lines and crosses.
• Work will include participating in cleaning and maintenance of equipment (e.g., butterfly cages, chambers, etc.)
• Assist in the analysis of results and the preparation of figures for publication/presentation.
• Aid in lab public outreach efforts.
• Assist in field expeditions for butterfly collections.

Skills: Butterfly Colony Care, Pest Management, Permit Management, Regulatory Compliance, Database Management, Equipment Maintenance, Data Analysis, Field Collection

• Assist Dr. Rosmarin and Dr. Kaufman in supervising the daily activities of research assistants, including contributing to performance evaluations.
• Collaborate with Dr. Rosmarin, implement and/or maintain an orientation and training program for all staff.
• Coordinate all (or a portion) of the research study activities.
• Act as a resource for all issues.
• Identify problems and develop solutions.
• Design, implement and evaluate recruitment strategies for study participants.
• Responsible for overseeing the data collection process.
• Ensure the integrity of patient data.
• Implement and maintain quality assurance procedures and systems.
• Collaborate with PI, develop and implement new research protocols, including design, data collection systems and IRB approval.
• Collaborate with Dr. Rosmarin and Dr. Kaufman, prepare and may present certain portions of presentations, in addition to preparing articles for publication.
• Responsible for monitoring grant budget, in collaboration with Dr. Rosmarin or Dr. Kaufman.

Skills: Staff Supervision, Training Coordination, Study Management, Problem Solving, Participant Recruitment, Data Integrity, Quality Assurance, Grant Budgeting

• Ensure that the conduction of assigned studies is in accordance with Good Clinical Practice, Federal regulations and institutional policies.
• Develop and maintain systems for the coding, editing, and computer entry of data for assigned research studies, focusing on continuous patient follow-up.
• Design and maintain management reports on the department and institutional databases for various research studies.
• Conduct research experiments and laboratory tests associated with specific protocols.
• Maintain research equipment.
• Evaluate and analyze data.
• Compile data and analyze results.
• Responsible for recording data in the methods requested.
• Assist the faculty investigator in data file preparation and attend data review meetings as required by the department.
• Prepare specific protocol reports and analysis to aid decisions regarding therapeutic efficacy and to assist in manuscript preparation and grant submissions.
• Attend departmental monthly meetings.
• Attend research team meetings.

Skills: Good Clinical Practice, Regulatory Compliance, Data Management, Laboratory Testing, Equipment Maintenance, Data Analysis, Research Reporting, Protocol Documentation

• Perform a variety of routine tests following established methodologies.
• Separate and quantify labeled and unlabeled lipids by TLC, GC, and HPLC (specific examples provided) as part of routine tests.
• Prepare and maintain tissue cultures.
• Prepare radioactive and non-radioactive samples for lipid analysis.
• Record data, summarize, and analyze results using basic statistics.
• Prepare laboratory reagents, chemicals, instruments, and equipment.
• Maintain supplies inventory in accordance with departmental procedures.
• Discuss the progress of work regularly with the supervisor.

Skills: Routine Laboratory Testing, Lipid Analysis, Tissue Culture, Sample Preparation, Data Analysis, Reagent Preparation, Inventory Management, Progress Reporting

• Work independently under general supervision, perform a variety of routine assays and experiments in the laboratory.
• Report on progress of work at lab meetings.
• Maintain supplies inventory in accordance with laboratory and department procedures.
• Place general orders for the lab in terms of common equipment.
• Assist in the orientation and training of new students, technicians, and fellows.
• Maintain established department policies, procedures and objectives, including the areas of quality assurance, safety, environmental and infection control.

Skills: Routine Assays, Independent Experimentation, Inventory Management, Lab Ordering, Staff Training, Quality Assurance, Safety Compliance, Progress Reporting

• Provide assistance to the Principal Investigator to coordinate clinical research activities related to the department's field of study and the investigator's specific study.
• Assist the research physician in the identification and follow-up of patients meeting criteria for inclusion in clinical research studies, ensuring protocol eligibility requirements are met.
• Establish and/or maintain a study record for each participant.
• Interview patient and/or family to explain the nature of the study, elicit cooperation and gather information to complete the study questionnaire.
• Facilitate obtaining informed consent.
• Schedule patient appointments and call patients to complete documentation.
• Review medical records to abstract information necessary to complete forms.
• Request and follow up on missing data, such as laboratory test results and the like.
• Monitor adherence to protocol, alert the physician when laboratory tests ordered have not been performed, medication protocol is not followed, etc.
• Perform research-based EKGs, vital signs, blood spinning and shipping of blood and tissue products in accordance with protocol specifications.
• Collect and organize patient data into an appropriate format to facilitate data entry.
• Operate the computer to enter study information into the database.
• Use pre-packaged software and, according to the needs of the research supervisor, perform computer-assisted statistical analysis such as multiple antecedent variables linear regression, frequencies, cross tabulations and the like.
• Write non-complex programs using a computer and software-compatible language to reformat information, create new files, etc.
• Maintain computer equipment, arrange for internal/external service to effect repairs and maintenance.
• Prepare related graphs and charts to report the results of the data gathered.
• Participate in quantitative and qualitative analyses of resultant information.
• Assist in planning research protocols.
• Coordinate the activities of others assigned to the research project to interview patients, complete forms, or perform other tasks.
• Review literature pertaining to research being conducted in order to better understand the project and gather relevant information.

Skills: Clinical Research Coordination, Patient Screening, Informed Consent, Patient Interviews, Medical Record Review, Clinical Testing, Data Management, Statistical Analysis

• Develop mathematically rigorous theory supporting the research objectives of the project.
• Develop, implement, and validate computational algorithms using a software package such as MATLAB.
• Document research findings through means of project reports and presentations.
• Communicate with investigators and other project participants regularly to report project progress and discuss potential issues/problems.
• Carry out experiments as instructed by PIRA will receive training to be able to perform the techniques required to complete the project.
• Gather, organize, enter and analyze data, perform literature searches on a computer and retrieve literature from the library.
• Make sure the lab environment complies with safety regulations.
• Attend weekly lab meetings, journal clubs and department seminars.

Skills: Mathematical Modeling, Algorithm Development, Computational Analysis, Research Documentation, Team Communication, Experimental Support, Data Analysis, Safety Compliance

• Able to create, highly motivated, adaptable, meticulous and well organised.
• Able to work independently and collaborate effectively in a highly diverse, multi-cultural and interdisciplinary team.
• Able to execute research projects to meet professional standards in terms of quality, timeliness and research outputs.
• Fluent in written and spoken English with good communication skills.
• Willingness to engage in deep learning in new areas.
• Experience in app development and peer-reviewed journal publications.
• Experience in mixed methods research and/or project execution involving human participants.
• Fluent in a second local language.

Qualifications: BS in Public Health with 5 years of Experience

• Previous experience with recruiting subjects and conducting focus groups, with an understanding of the ethical and technical conduct of research, and volunteer management experience.
• Excellent English communication skills (oral and written).
• Bilingual or multi-lingual skills (beyond that of English) to the patient population served.
• Demonstrated history of cultural sensitivity and comfort with a wide range of social, racial and ethnic populations.
• Must have prior exposure to tools such as REDCAP, EPIC (Electronic Medical Record), BOX, Microsoft Office, Outlook Calendars, Zoom, and G Suite.
• Must have prior engagement with epilepsy-specific projects or related communities.
• Experience with data analysis tools such as NVIVO, R and/or SAS.
• Strong familiarity with HIPAA, must be able to maintain strict confidentiality of all personal/health sensitive information.
• Must exercise strong interpersonal skills, high attention to detail and an ability to build rapport with patients and professionals from diverse backgrounds.

Qualifications: BS in Biology with 4 years of Experience

• Experience with recruiting subjects, with an understanding of the ethical and technical conduct of research.
• Excellent English communication skills, both written and oral.
• Must have bilingual or multi-lingual skills (beyond that of English) appropriate to the patient population served.
• Able to demonstrate cultural sensitivity and comfort with a wide range of social, racial and ethnic populations.
• Organizational ability to perform multiple tasks efficiently and to prioritize duties.
• Must show excellent attention to detail.
• Proficient with Microsoft Office applications, including Word, Outlook, Excel, and Access and PowerPoint.
• Experience with statistical analysis tools.
• Ability to perform basic data management tasks (coding, data entry, data cleaning, retrieval).
• Ability to perform basic data analysis and reporting (in words, numbers and graphics).
• Experience using quantitative data analysis software (e.g., SPSS, SAS, Minitab).
• Excellent interpersonal skills, work with human subjects and patients in a hospital setting.
• Must be able to maintain strict protocols for all confidential or sensitive information.
• Experience with Google Drive, WordPress, and GoToWebinar/GoToMeeting.

Qualifications: BA in Sociology with 3 years of Experience

• Strong oral/written language and investigative skills.
• Ability to prioritize assignments, multitask, make decisions based upon sound principles and independently problem solve.
• Ability to manage multiple projects simultaneously, including both long-term and short-term projects.
• Excellent interpersonal and organizational skills.
• Ability to work both independently as well as with a team.
• Must have skill at using Microsoft Excel, PowerPoint, and Word.
• Must possess well-developed computer skills.
• Experience with medical imaging data is a strength.
• Excellent analytical skills and strong oral/written communication skills.
• Excellent attention to both detail and process.
• Ability to respect the strict confidentiality of medical records and study data.
• Ability to respond to changing goals and priorities in a fast-paced and dynamic start-up environment.

Qualifications: BA in Behavioral Science with 4 years of Experience

• Fluent in at least one Ethiopian language/Amharic and either Afar or Tigrinya.
• Fluent in English, written and spoken.
• Previous experience in data collection, including analysis and write-up.
• Understanding of the Ethiopian health systems.
• Strong interpersonal and communication skills.
• Experience and ability to work in fragile contexts.
• Good understanding of the work environment and a critical ethical consideration in the data collection process.
• Experience using digital data collection tools (RedCap).
• Must have a high level of integrity and respect for research confidentiality.
• Able to adhere to all project data protocols and be responsible for maintaining good relations with the NIIDS team, partner organizations, and project participants.
• Willingness to learn, explore new experiences, and work in remote settings.
• Able to participate in the training of the team with full attendance and participation.
• Able to participate and present the results in a consultative meeting (debriefing).
• Previous experience of working with women and adolescents.

Qualifications: BA in Health Studies with 3 years of Experience

• Experience working with research study protocols.
• Able to detail-oriented manner with close attention to accuracy.
• Must demonstrate basic computer skills.
• Strong written and verbal communications.
• Ability to develop rapport with a diverse pool of research participants.
• Ability to navigate sensitive topics and maintain the confidentiality of participants.
• Ability to collaborate within multi-disciplinary team settings.

Qualifications: BS in Chemistry with 1 year of Experience

• Prior experience working with subjects/patients and working on a research team.
• Computer program proficiency (Microsoft Office Suite).
• Ability to work independently in a busy, research, academic, open office setting with other employees.
• Excellent organizational skills and ability to prioritize a variety of tasks.
• Good attention to detail.
• Excellent interpersonal skills.
• Good oral and written communication skills.
• Working knowledge of computer programs, databases, etc.
• Ability to learn new skills and procedures quickly and perform them independently.
• Ability to demonstrate professionalism and respect for subject rights and individual needs.
• Must be able to be HIPAA compliant at all times.

Qualifications: BA in Anthropology with 2 years of Experience

• Able to lift and carry 20-50 lbs of weight.
• Able to complete repetitive motions with wrists and hands, stand, walk for prolonged periods, stoop, bend, kneel, crouch, with or without reasonable accommodations.
• Able to work in warm conditions and in variable environments, including partially enclosed structures.
• Ability to read and communicate in Spanish and work in a team of diverse cultural backgrounds.
• Fluent in reading and writing English.
• Basic mathematics and computer skills.

Qualifications: BS in Biomedical Engineering with 1 year of Experience

• Experience with microscopes and basic laboratory equipment.
• Experience with ''wet'' laboratory techniques.
• Organizational skills and basic computer skills.
• Record-keeping experience.
• Must have an interest in science and medicine.
• Effective communication skills.
• Ability to work independently and ask appropriate questions.
• Ability to learn new software and technology.
• Experience with processing imaging data.

Qualifications: BA in Political Science with 2 years of Experience

• Must have careful attention to detail.
• Good organizational skills.
• Ability to follow directions.
• Good communication skills.
• Must have computer literacy.
• Working knowledge of clinical research protocols.
• Ability to demonstrate respect and professionalism for subjects’ rights and individual needs.

Qualifications: BS in Environmental Science with 1 year of Experience

• Experience with health data and statistical analysis in a research environment.
• Solid statistical knowledge and experience using statistical software packages (such as SAS, R, or Stata), and programming languages.
• Able to organize, resourceful and self-starting with meticulous attention to detail.
• Comfortable in communicating with the research community.
• Excellent verbal and written communication skills.
• Proven ability to work in a team setting.
• Able to handle multiple and competing priorities.
• Proficient in Adobe Pro and Microsoft Office (Word, Excel, and Outlook).

Qualifications: BS in Statistics with 3 years of Experience

• Must have the ability to perform multiple tasks and prioritize duties.
• Ability to work independently.
• Must possess excellent interpersonal, verbal and written communication skills.
• Must have an interest in performing new and varied work assignments, and be flexible with regard to work assignments.
• Extensive knowledge of Microsoft Excel, Access, PowerPoint and Word.
• Knowledge or ability to learn Minitab.
• Must have the ability to maintain confidentiality.

Qualifications: BA in Sociology with 2 years of Experience

• Research or administrative experience, an investment or financial services firm.
• Ability to communicate and work in a team environment, meet deadlines, and work in a fast paced.
• Able to environment and manage multiple projects.
• Strong organizational, written communication skills.
• Must have detail-oriented, excellent interpersonal, analytical and judgment skills.
• Ability to self-starter and self-motivated.
• Proficient with Microsoft Office, including advanced proficiency in Excel and Outlook.

Qualifications: BS in Public Health with 3 years of Experience

• Must have skill in completing assignments accurately and with attention to detail.
• Ability to analyze, organize and prioritize work under pressure while meeting deadlines.
• Ability to process and handle confidential information with discretion.
• Ability to work evenings, nights, and weekends.
• Ability to work independently and/or in a collaborative environment.

Qualifications: BS in Neuroscience with 2 years of Experience

• Experience in clinical studies and training in Good Clinical Practice.
• Good written and communication skills.
• Able to interact well with patients and clinicians.
• Able to work meticulously, independently and as a team player.
• Must have computer proficiency, MS Word, PowerPoint and Excel.

Qualifications: BA in Political Science with 1 year of Experience

• Excellent skills with organization, prioritization and time management, attention to detail, collaboration, and multi-tasking.
• Strong written and verbal communication skills, professional presence, and outstanding interpersonal skills.
• Knowledge of Microsoft Office, particularly experience with Excel.
• Experience with data analytic programs (e.g., SPSS, R).
• Experience with survey platforms (e.g., Survey Monkey, Qualtrics).
• Able to team player with a positive attitude.
• Past research experience.
• Must be bilingual in Spanish.

Qualifications: BA in Behavioral Science with 2 years of Experience

• Experience using data collection apps or software.
• Experience with data entry tools and working with quantitative and/or qualitative data sets.
• Experience using statistical software and/or qualitative data analysis software.
• Tobacco control-related knowledge and experience.
• Fluent in Hindi, Bangla, Urdu, Bahasa Indonesia, Spanish, Portuguese, Chinese, Vietnamese, Tagalog, Russian, or Ukrainian.
• Exceptional attention to detail.
• Strong organizational skills.
• Strong oral and written communication skills.
• Ability to work well in a team and independently.

Qualifications: BS in Statistics with 3 years of Experience

• Excellent skills in synthetic organic chemistry, ideally also in polymer chemistry.
• Ability to plan and accurately document practical work.
• Must have a safety-first attitude, comply with process safety best practices.
• Must have a hands-on attitude, problem-solving skills, positive mindset and good communication and teamwork skills.
• Ability to organize and tidy personality.
• Ability to bring flexibility for changing work assignments.
• Fluent in English, both written and oral, German.

Qualifications: BS in Neuroscience with 4 years of Experience

• Must have certification in the protection of human research subjects (can be obtained after hire).
• Must have competency in Microsoft Word, PowerPoint, and Excel.
• Experience with data management, including using word-processing, spreadsheet, MS Access database software, REDCap and EndNote.
• Strong familiarity with videoconference equipment and webinar setup.
• Excellent interpersonal skills, working with hospital leadership and study staff.
• Ability to demonstrate professionalism and respect.
• Good oral and written communication skills.
• Must respect patient privacy.
• Strong work ethic, industrious.
• Organizational skills and ability to prioritize tasks.
• Ability to complete work and to meet deadlines.
• Must have competency with Microsoft Word, PowerPoint, Excel and Access.
• Ability to use medical bibliographic retrieval programs.

Qualifications: BS in Biology with 3 years of Experience

• Agricultural or horticultural experience.
• Ability and willingness to be a pesticide handler.
• Ability to work independently and problem solve.
• Able to occasionally lift, push, or carry up to 50 lbs of weight.
• Able to complete repetitive motions with wrists and hands, stand, walk for prolonged periods, stoop, bend, kneel, or crouch, with or without reasonable accommodations.
• Able to work in warm and cold conditions and in variable environments.
• Ability to read and communicate in English and work in a team of diverse cultural backgrounds and languages.
• Must have basic mathematics.

Qualifications: BS in Chemistry with 2 years of Experience

• Excellent conversational and business English (written and oral).
• Solid track record of extra-curricular achievement.
• Strong commitment to high-quality work and an interest in rapid learning and skill development.
• Proven analytical, interpretative and problem-solving skills.
• Strong interpersonal and relationship-building skills and an ability to build credibility with external and internal contacts.
• Good commercial awareness/business judgement and an interest in the healthcare industry.

Qualifications: BA in Anthropology with 1 year of Experience

• Experience in clinical research, public health experience, or working with children under age 6.
• Experience working directly with youth with disabilities and their families and/or support persons.
• Experience in outreach, communication, and relationship building within a variety of populations, and past group leadership of some kind.
• Previous experience with recruiting subjects, with an understanding of the ethical and technical conduct of research.
• Excellent English communication skills (oral and written).
• Must have bilingual or multi-lingual skills (beyond that of English) appropriate to the patient population served.
• Must have cultural sensitivity and comfort with a wide range of social, racial and ethnic populations.
• Proficient with Microsoft Office applications (i.e., MS Word, Excel, Access, PowerPoint, Outlook) and web browsers.
• Previous experience with data analysis and statistical software, including SAS, R, and/or NVIVO.
• Must be able to maintain strict confidentiality of all personal/health sensitive information.

Qualifications: BA in Sociology with 5 years of Experience

• Previous experience working as an administrator in an office environment.
• Must have a passion for working in a fast-moving, dynamic environment.
• Excellent customer service and teamwork skills.
• Must have  MS Office skills (Word, Excel and Outlook).
• Good oral and written communication skills.
• Fluent in Polish and good command of the English language.

Qualifications: BS in Statistics with 1 year of Experience

• Prior experience with clinical research and interaction with human subjects.
• Ability to familiarize with basic data management techniques, including statistical packages (e.g., SPSS) and Excel.
• Excellent organizational and analytic skills.
• Excellent interpersonal skills, working with the study participants.
• Excellent oral and written communication skills.
• Ability to prioritize tasks and work independently.
• Knowledge of basic principles of psychology, cognitive neuroscience, and clinical research.
• Knowledge of data management and statistical programs.
• Ability to demonstrate professionalism and respect for the rights and needs of study participants.
• Able to facility with managing and adapting projects in the REDCap research database, or experience with other electronic data capture (EDC) systems of electronic health records (EHR).

Qualifications: BS in Computer Science with 4 years of Experience

• Experience with iPSC culture and/or differentiation.
• Ability to practice in gene editing processes such as CRISPR/Cas9.
• Ability to be flexible in day-to-day activities to accommodate changes in priorities and lab duties.
• Must have sufficient command of the English language to understand protocols and assigned tasks, communicate results and record lab notebooks in English.
• Able to self-motivated, detail-oriented and systematic approach to work in general.
• Able to team-oriented, responsible and reliable personality.

Qualifications: BS in Biology with 3 years of Experience

• Proficient in Microsoft Office Suite, including Word, Excel, PowerPoint, and Outlook.
• Strong written and verbal communication and interpersonal skills.
• Ability to work independently and as part of a team.
• Strong administrative ability.
• Strong organizational skills.
• Able to complete tasks in a timely fashion.
• Understanding and ability to utilize a variety of computer software and hardware across a variety of platforms.

Qualifications: BS in Chemistry with 1 year of Experience

• Knowledge of commonly-used concepts, practices, and procedures within molecular biology and tissue culture skills (PCR, Immunoblot, Retroviral/Lentiviral production).
• Ability to operate laboratory equipment.
• Ability to meet consistent attendance.
• Ability to interact with colleagues, supervisors and customers face-to-face.
• Previous experience working with animals.
• Must demonstrate compliance with university animal research and care (ARC) policies and procedures and compliance with regulations of the Animal Welfare Act, Public Health Service Policy, AAALAC guidelines and other applicable regulatory guidelines.
• Must handle animals with care and respect at all times.
• Must be able and willing to learn new techniques, procedures, processes, and computer gear to protect the health of the animals.

Qualifications: BA in Sociology with 2 years of Experience

• Must be able to read and write English, and communicate clearly with staff and participants.
• Able to accuracy and attention to detail.
• Must have superior organizational skills.
• Ability to identify and follow through on project issues, show initiative, and operate independently and with good judgment.
• Ability to exhibit professionalism in all aspects of job performance.
• Excellent oral and interpersonal communication skills.
• Basic computer and keyboard skills.

Qualifications: BA in Anthropology with 1 year of Experience

• Efficient with Microsoft Word, Excel, PowerPoint, and Adobe Photoshop.
• Able to communicate effectively in both written and oral formats.
• Able to innovate and problem-solve.
• Ability to mentor volunteer students.
• Demonstrated evidence of strong written and verbal communication skills.
• Ability to manage competing priorities.
• Ability to meet deadlines and urgent system needs.
• Ability to work independently, willingness to serve as a positive and professional role model.
• Must have demonstrated a record of reliable attendance, punctuality and proven successful performance in past and present.

Qualifications: BS in Computer Science with 2 years of Experience

• Prior experience with clinical research and interaction with human subjects.
• Strong familiarity with basic data management techniques, including statistical packages (e.g., SPSS) and Excel.
• Experience with database design/development.
• Excellent interpersonal skills are required for working with the study participants.
• Knowledge of basic principles of psychology and cognitive neuroscience.
• Knowledge of clinical research protocols.
• Knowledge of computer programs, databases, etc.
• Excellent organizational skills and ability to prioritize a variety of tasks.
• Ability to pay attention to detail.
• Good oral and written communication skills.
• Ability to demonstrate professionalism and respect for subjects' rights and individual needs.

Qualifications: BA in Political Science with 3 years of Experience

• Knowledge of basic lab techniques, including pipetting, staining, culture techniques and aliquoting.
• Able to perform basic lab maintenance tasks.
• Understanding of quality control.
• Understanding of safety practices related to work performed.
• Must have skill in the use of computer software related to research needs.
• Able to instruct others in lab and safety protocols.

Qualifications: BA in Psychology with 1 year of Experience

• Experience to become familiar with specific research studies.
• Knowledge of theory and techniques of research methodology.
• Must have organizational skills to organize and prioritize own efforts on multiple projects and to gather research information format appropriate for computer data entry, prepare and maintain records and reports, etc.
• Must have interpersonal skills to effectively interact with patients, families and Hospital professionals to gather and exchange information.
• Must have analytical skills to participate in developing research protocols, perform statistical analyses and participate in qualitative/quantitative analyses of research data.
• Must have the technical ability to operate and maintain the computer system.
• Demonstrated knowledge and skills to provide care to patients with consideration of aging processes, human development stages and cultural patterns in each step of the care process.

Qualifications: BS in Neuroscience with 3 years of Experience

• Must be fully bilingual in spoken and written English and Spanish.
• Experience with research concepts and techniques, including qualitative interviewing and quantitative analysis.
• Must have talent for multitasking and an aptitude for thinking on numerous levels simultaneously.
• Must have a reliable car (mileage reimbursement provided).
• Ability to work a flexible schedule, including some evenings and weekends, to support staff and events and be on call.
• Ability to function autonomously in a collaborative interdisciplinary team involving research, medical and mental health care.
• Excellent written and verbal communication and interpersonal skills.
• Demonstrated strong administrative skills and a strong attention to detail.
• Strong computer skills.
• Ability to work harmoniously with diverse groups of individuals.
• Experience working in an ethnically, culturally and racially diverse environment.

Qualifications: BA in Political Science with 4 years of Experience

• Good interpersonal and communication skills.
• Good organizational skills, detail-oriented.
• Ability to methodically record data and to analyze data using basic statistics.
• Ability to perform a variety of routine tests and prioritize work.
• Knowledge of computer programs, databases, etc.
• Ability to demonstrate professionalism.

Qualifications: BS in Chemistry with 2 years of Experience

• Must have prior experience working with human subjects.
• Able to write a sample (e.g., honors thesis, manuscript, essay).
• Experience conducting psychological or neuroscience research.
• Must have a high degree of computer literacy (e.g., Excel, Word).
• Ability to pay attention to detail and conscientiousness.
• Excellent organizational and time management skills, including the ability to prioritize a variety of tasks.
• Ability to work independently and problem-solve.
• Excellent interpersonal skills are required for working with study participants.
• Good oral and written communication skills.
• Must have professionalism, ethical behavior, and respect for subjects’ rights, confidentiality, and individual needs.
• Must be able to consistently demonstrate McLean Values of integrity, compassion and respect, diversity and teamwork, excellence and innovation.

Qualifications: BS in Environmental Science with 3 years of Experience

• Ability to work independently, with minimal supervision.
• Excellent verbal and written communication skills.
• Demonstrated organizational skills.
• Must have close attention to detail.
• Previous experience with chart abstraction and data entry.
• Previous experience with MiChart or other Electronic Health Records.
• Experience with Qualtrics, RedCap, and Excel, or other electronic data entry and management software.
• Proficient in the Microsoft suite.
• Knowledge of medical terminology.
• Prior human subjects research experience.

Qualifications: BS in Statistics with 2 years of Experience

• Experience as a software developer, preferably in the high-performance computing sector, hardware design and characterization.
• Must be conversant in C/C++, Python and Java.
• Experience with FPGA RFSoC programming using Verilog/VHDL for Xilinx and/or Altera devices.
• Experience in phase-coherent RF signal design.
• Good communication skills and ability to perform research in a collaborative environment, in synergy with other developers and researchers.

Qualifications: BS in Computer Science with 4 years of Experience

• Demonstrated experience in entering data into and managing research databases according to best practice.
• Demonstrated ability to acquire new skills.
• Excellent interpersonal, written and verbal communication skills.
• Demonstrated a high level of organization with careful attention to detail.
• Prior research experience in a related field.
• Experience working with research subjects.
• Experience with programming.
• Strong familiarity with brain imaging (MRI, CT, EEG).
• Demonstrated coursework and aptitude in statistics (SPSS, GraphPad Prism).

Qualifications: BA in Psychology with 3 years of Experience

• Able to organize, self-motivated, empathic, personable, professional, and efficient and has strong communication skills.
• Able to work independently for extended periods while maintaining effective communication with team leads, study coordinators and principal investigators.
• Able to prioritize multiple tasks, meet deadlines, and adhere to strict confidentiality policies.
• Previous clinical research experience, clinic/hospital work, or volunteer experience, and knowledge of the research process.
• Experience working on a multi-disciplinary team and using MiChart and Qualtrics.

Qualifications: BA in Sociology with 2 years of Experience

• Professional work experience with one or more of the following user research methods, semi-structured interviews, surveys, usability studies (either live or remote), concept validation, cognitive walkthroughs, surveys (creation and analysis).
• Effective interpersonal, negotiation and collaboration skills.
• Ability to prioritize time between multiple projects, and be flexible by adapting to changing schedules and different projects.
• Knowledge of the business environment.
• Good command of Microsoft Office.
• Good communication skills in English, both oral and written.
• Must have bilingualism in French and English.

Qualifications: BS in Computer Science with 3 years of Experience

• Excellent verbal and written communication skills.
• Excellent interpersonal skills, including the ability to work effectively and efficiently in a team.
• Understanding of and commitment to UNSW’s aims, objectives and values in action, together with relevant policies and guidelines.
• Knowledge of health and safety responsibilities and commitment to attending relevant health and safety training.
• Experience preparing Next-Gen sequencing libraries, loading Illumina flow cells, and running sequencing instruments.
• Experience and demonstrated ability using pipettes.
• Proven ability to follow protocols to run assays, formulate and prepare scientific solutions and media.

Qualifications: BS in Neuroscience with 2 years of Experience

• Experience and knowledge in human blood sample processing and cell cryopreservation techniques, cell culture methods, and cellular staining procedures using flow cytometry.
• Knowledge and understanding of working in a GLP/GCP compliant regulatory laboratory to conduct experimental procedures per defined technical SOPs, with experience in handling biohazardous materials, and understanding safety procedures and guidelines.
• Ability to handle a relatively high volume of clinical sample processing and analysis, using immunoassay techniques.
• Good organizational and documentation skills.
• Good programming and analytical skills.
• Highly proficient with MS Office (Word, Excel, Outlook), email, and the internet.

Qualifications: BA in Political Science with 4 years of Experience

• Able to work well in a team while being a self-starter.
• Ability to maintain a positive attitude.
• Ability to prioritize tasks.
• Proficient in Microsoft Office, including Excel and Word.
• Excellent organizational, time management skills.
• Experience writing code in R and Python.
• Able to familiarize with epidemiology/economics.
• Experience with data analysis and machine learning.

Qualifications: BS in Chemistry with 2 years of Experience

• Able to analyze and interpret data and meet deadlines.
• Able to follow oral and written instructions and established procedures.
• Able to maintain accuracy and consistency, and conduct themselves ethically.
• Able to work as an effective team member, dealing calmly and courteously with people and with excellent verbal communication skills.
• Experience in a working laboratory environment, preferably within the Medical Device/Pharmaceutical Industry.
• Knowledge and understanding of compliance with FDA and European regulations relating to Quality Systems (ISO13485:2003, ISO9001:2000, FDA 21 CFR part 820) and GMP Guidelines and Regulations.
• Good working knowledge of Microsoft Office, specifically Word and Excel.

Qualifications: BS in Biology with 3 years of Experience

• Experience conducting qualitative research in Singapore.
• Able to organise, detail-oriented and motivated to learn.
• Demonstrated interest in issues related to smart cities, platform urbanism, urban development, urban infrastructure, and Southeast Asia.
• Must have language skills in Thai or Bahasa Indonesia.
• Demonstrated ability to accurately collect, store and interpret research data.
• Demonstrated ability to communicate with patients, staff, and investigators.

Qualifications: BA in Psychology with 2 years of Experience

• Must have evidence of Research in a relevant mental health discipline, ideally child mental health research.
• Experience conducting clinical assessments or interviews with people with mental health concerns.
• Experience working with clinical teams in a clinical or research context.
• Experience in writing grant applications.
• Must have and use strong overall organizational skills, customer service skills, public relations skills, and time management skills.
• Excellent written and verbal communication skills, the ability to be detail-oriented and interact effectively with all levels (i.e., doctors, patients, vendors, peers, staff, and management).

Qualifications: BS in Environmental Science with 3 years of Experience

• Must have an interest in developing vaccines and therapeutics against emerging infectious diseases.
• Strong interpersonal communication skills with written, oral communication and computer skills.
• Proficient in working with mosquitoes and molecular biology.
• Able to team player who is open-minded, energetic, highly motivated and can work collaboratively in an interdisciplinary team and diverse workforce.
• Ability to work as part of a team.
• Good communication.
• Able to critically.
• Must have organisational skills.

Qualifications: BA in Political Science with 2 years of Experience

• Strong written and verbal communication skills.
• Ability to manage multiple projects in a timely manner.
• Ability to build relationships, collaborate and work on teams.
• Ability to set and meet deadlines for oneself.
• Proficient in Microsoft Office and Adobe software suites.
• Previous research experience working with human subjects.
• Must have base on the area of assignment bilingual skills.

Qualifications: BS in Statistics with 1 year of Experience

• Knowledge of ELISA (enzyme-linked immunosorbent assay).
• Experience working in a BSL-2 certified lab.
• Experience handling/processing blood and infectious diseases.
• Proficient in Excel and Word.
• Experience with single and multi-channel pipettes.
• Excellent attention to detail, flexibility, strong communication skills, and a team-player attitude.

Qualifications: BA in Sociology with 2 years of Experience

• Basic computer skills, including standard software, including the Microsoft Office suite.
• Experience with RedCap software.
• Experience with Freezerworks software.
• Basic laboratory skills.
• Must have writing and verbal communication ability.
• Intermediate proficiency with Microsoft Excel, Word, and PowerPoint.

Qualifications: BS in Biology with 1 year of Experience