CLINICAL RESEARCH COORDINATOR SKILLS, EXPERIENCE, AND JOB REQUIREMENTS

Updated: Jun 27, 2025 - The Clinical Research Coordinator has experience in clinical research protocols and trials with strong expertise in clinical data management, database operations, and regulatory compliance, including IRB and FDA standards. This role requires certification in GCP, HSP, CPR, and CCRP or LVN/RN credentials, with excellent decision-making, writing, and accountability skills. The coordinator also demonstrates resilience, energy, and adaptability in communication, teamwork, and overcoming challenges.

Essential Hard and Soft Skills for a Standout Clinical Research Coordinator Resume
  • Trial Coordination
  • Project Tracking
  • Data Management
  • Data Entry
  • Quality Assurance
  • Study Implementation
  • Survey Coordination
  • Regulatory Documentation
  • Site Management
  • GCP Compliance
  • Ethical Recruitment
  • Teamwork
  • Relationship Building
  • Participant Enrollment
  • Subject Recruitment
  • Site Coordination
  • Stakeholder Communication
  • Stakeholder Engagement
  • Problem Solving
  • Adaptability

Summary of Clinical Research Coordinator Knowledge and Qualifications on Resume

1. BS in Pre-Medicine with 1 year of Experience

  • Previous coordinator experience and CCRC Certification
  • Open and clear communication skills
  • Excellent written and verbal communication skills
  • Detailed and able to meet strict key deadlines
  • Team player with a positive attitude
  • Hold an LPN or RN
  • Must practice discretion and adhere to hospital confidentiality guidelines at all times.
  • Must have computer skills, including the use of the Microsoft Office Suite

2. BS in Public Health with 3 years of Experience

  • Prior experience working in healthcare.
  • Expertise or prior experience in the clinical area applicable to this research role (i.e., cardiology, pulmonary, oncology, women and newborn, etc.
  • Clinical research experience working with human subjects.
  • Professional certifications such as the CCRP (Certified Clinical Research Professional- SoCRA), CCRC (Certified Clinical Research Coordinator - ACRP), CIRB (Certified Institutional Review Board professional), or CRA (Certified Research Administrator)
  • Experience using basic computer programs, including word processing, database, spreadsheet applications, and e-mail.
  • Experience using laboratory protocol, systems, and documentation techniques.
  • Excellent organization and communication skills
  • Strong interpersonal skills with the ability to effectively interact with all levels of staff and external contacts.
  • Must be detail-oriented and have the ability to follow through.

3. BS in Nursing with 2 years of Experience

  • A strong background in Life Sciences or Nursing
  • Working experience as CRC
  • Knowledge of venepuncture/cannulation
  • Good time management and communication skills
  • Able to work independently and detail-oriented
  • Must have computer literacy
  • Ability to effectively manage time and prioritize workload.

4. BS in Clinical Research with 5 years of Experience

  • Experience in clinical research or a related field.
  • Knowledge of clinical quality management and systems (such as Veeva, Master Control, etc.)
  • Excellent communication, grammar, and writing skills
  • Superior knowledge of research protocols and clinical, scientific, and/or medical terminology.
  • Demonstrated superior experience with data collection.
  • Demonstrated experience with Microsoft Office (Word, Excel, etc.).
  • Excellent organizational skills
  • Good communication skills, both verbal and written

5. BS in Biology with 3 years of Experience

  • Relevant experience in hospitals or medical surgery
  • Knowledge of ICH-GCP Guidelines and the PAREXEL internal Operating Procedures (SOPs)
  • Good English knowledge
  • Advanced computer skills (Windows Office)
  • Have strong organizational talent
  • Ability to work under pressure and flexibility in working times
  • Ability to work on weekends and holidays

6. BS in Pharmacology with 4 years of Experience

  • Prior experience coordinating drug and device clinical trials.
  • Experience with oncology or hematology studies.
  • Clinical research, scientific or medical experience
  • Excellent communication, decision-making, and problem-solving skills.
  • A proven capacity to set priorities for teams, coordinate multiple assignments, work in a fast-paced, multi-tasked environment, and exercise sound judgment in setting priorities.
  • Experience with project management software and MS Excel, Smartsheet, RedCap, or other database programs.
  • Experience in clinical research, or an equivalent combination of education and relevant experience.
  • Strong interpersonal skills
  • Proficiency with Microsoft Office and database applications.
  • Experience with research protocols and regulatory or governing bodies, which include HIPAA and FDA regulations, Institutional Review Board requirements, and Good Clinical Practices.
  • Knowledge of medical terminology.

7. BS in Healthcare Administration with 1 year of Experience

  • A strong background in life sciences
  • Prior experience with patient interaction, human research, and/or the IRB
  • Extraordinary interpersonal skills and ability to work as part of a multidisciplinary team.
  • Ability to comfortably and sensitively interact with study participants, as well as work independently as well as a member of the team.
  • Superb organizational skills with the ability to multitask, take initiative, and prioritize tasks.
  • Excellent attention to detail and ability to document research activities.
  • Excellent writing and communication skills in the English language.
  • Excellent problem-solving skills.
  • Computer literacy as it relates to Microsoft Windows environments, including the ability to troubleshoot simple computer problems independently.
  • Ability to safeguard the privacy of information and keep appropriate information confidential.

8. BS in Health Information Management with 3 years of Experience

  • Relevant work experience in a clinical environment or equivalent combination of education, training, and experience
  • Working knowledge of clinical trials and Good Clinical Practices (GCP)
  • Skill in carrying out clinical procedures such as intravenous catheter insertion and spirometry testing
  • Good skill in using MS Windows and Office applications such as Access, Outlook, and Word
  • Ability to establish and maintain effective working relationships with coworkers, managers, and clients
  • Ability to demonstrate respect and professionalism for subjects’ rights and individual needs

9. BS in Microbiology with 2 years of Experience

  • Clinical Research Coordinator certification 
  • Previous clinical research coordination experience
  • Effectively uses Microsoft computer software
  • Demonstrates ability to coordinate and establish priorities among diverse tasks
  • Effectively communicates verbally and in writing
  • Careful attention to details

10. BS in Pharmacology with 3 years of Experience

  • Experience in pharma and/or biotech clinical research
  • Experience and knowledge in document management
  • Knowledge of the clinical trial process.
  • Knowledge of ICH guidelines and GCP, including a basic understanding of regulatory requirements
  • Understanding of the regulatory progression of establishing and maintaining clinical sites
  • Advanced Microsoft Office Word, Excel, and PowerPoint

11. BS in Health and Human Services with 2 years of Experience

  • A strong background in a scientific, health-related, or business administration program
  • Previous clinical research experience.
  • Licensed as a practical nurse (LPN)
  • Working knowledge of clinical research protocols
  • The ability to follow directions
  • Strong organizational and communication skills

12. BS in Epidemiology with 4 years of Experience

  • Progressively responsible related experience coordinating clinical/research trials and studies.
  • Proficiency in using various Microsoft Office applications such as Word, Excel, Access, PowerPoint, and Outlook.
  • Familiar with Internet applications.
  • Effective oral, written communication, and interpersonal skills.
  • Ability to interface effectively with all levels of management and must work and communicate effectively with both internal and external customers.
  • Ability to work within a team environment as well as independently as well as work and make decisions independently.
  • Time management skills and the ability to multitask.
  • Strong understanding and knowledge base of coordination requirements associated with clinical/research trials.
  • Ability to identify, analyze, and solve problems with the ability to work well under pressure.

13. BS in Allied Health with 1 year of Experience

  • Someone with relevant course/project work or those without any prior research experience considered for the Clinical Research Coordinator I position
  • Directly related work experience for a Clinical Research Coordinator II position.
  • Strong interpersonal skills and the ability to interact professionally with study participants and other members of the research team
  • Meticulous attention to detail
  • Initiative and motivation to work hard
  • Ability to prioritize competing demands
  • Work independently with very little guidance from supervisors.

14. BS in Clinical Laboratory Science with 3 years of Experience

  • Experience working in a clinic as an MA or in other roles with patient-facing interaction
  • Phlebotomy and Dermatology experience 
  • Excellent interpersonal communication skills
  • The ability to exercise empathy when working with patients and their families
  • Strong organizational and time management skills
  • Demonstrate an understanding of clinical procedures, laws, and regulations
  • Extensive knowledge of medical terminology
  • Must possess the ability to work independently and display initiative to introduce innovations to the research study.

15. BS in Health Informatics with 5 years of Experience

  • Experience in clinical operations or a related field
  • Knowledge of drug development, clinical operation processes, and documentation, including study start-up procedures, maintenance phase, and study close-out procedures.
  • Knowledge of Neuroscience/CNS/Psychiatric clinical research.
  • Knowledge of ICH/GCP and regulatory environments, including regulatory documentation review and approval.
  • Knowledge and implementation of the processes involved in clinical studies following Good Clinical Practice (GCP) and the Code of Federal Regulations
  • A broad understanding of essential study documentation
  • Experience with eTMF with the ability to directly apply essential document knowledge to file documents accordingly based on the TMF reference model.
  • Strong communication and interpersonal/team skills.
  • Proficient in MS Excel, Word, and PowerPoint. Knowledge of MS Project
  • Established ability to prioritize and manage multiple tasks simultaneously, demonstrated ability to identify and resolve issues, and effectively manage timelines.
  • Strong initiative and a can-do attitude, excellent organizational skills
  • Proven effectiveness in a quick-changing, fast-paced environment, excellent people skills, and a proven record as a team player.

16. BS in Biology with 8 years of Experience

  • Experience conducting clinical trials, worked as primary research coordinator for at least 5 drug or device trials.
  • Experience interacting with patients in a healthcare setting
  • Thorough knowledge and understanding of research regulatory requirements involving human subjects research, including FDA, OHRP and GCP requirements
  • Experience in the implementation of research protocols and clinical trials processes
  • Experience in preparing and maintaining regulatory documents and other IRB-related study documentation
  • Experience using electronic data capture software and Clinical Trial Management Systems (CTMS)
  • Experience with Microsoft Office software 
  • Knowledge of medical terminology
  • Working experience with lab processing
  • Current certification (CCRP or CCRC) by the Society of Clinical Research Associates (SOCRA) or Association of Clinical Research Professionals (ACRP), or obtained within the first year in the role.
  • Current certificate of Human Subjects Protection and Good Clinical Practice training within the first six months on the job.
  • Phlebotomy certification, BLS and First Aid Certification, IATA and/or Safe-T-Pak Certification for shipment of lab specimens and/or dry ice
  • Experience working in IDX EMR
  • Must have strong analytical skills and conceptual thinking.
  • Ability to resolve technical problems and interpret the acceptability of data results.

17. BS in Pre-Medicine with 1 year of Experience

  • Medical terminology, knowledge of disease processes and anatomy, and oncology
  • Working knowledge of regulatory requirements
  • Attention to detail and accuracy
  • The ability to meet deadlines
  • Excellent interpersonal skills
  • Excellent written and oral communication skills
  • The ability to travel to local/regional offices

18. BS in Biochemistry with 4 years of Experience

  • Experience as a Clinical Research Coordinator, Study Coordinator, Data Manager, or similar role in clinical research.
  • Working knowledge of Good Clinical Practice guidelines and Federal research regulations.
  • Strong understanding and knowledge base of coordination requirements associated with industry-funded clinical trials.
  • Demonstrated strong organizational and communication skills.
  • Must be comfortable communicating clinical information to medical personnel.
  • Proven organizational skills, including attention to detail and multi-tasking skills
  • Ability to work within a team environment as well as independently
  • Ability to identify, analyze, and solve problems while working under pressure
  • Strong computer literacy

19. BS in Biotechnology with 3 years of Experience

  • Experience as a CRC, preferably with practice coordinating industry-sponsored vaccines in a private setting.
  • Be an energetic, go-getter who is detail-oriented and can multitask.
  • Be goals-driven while continuously maintaining quality.
  • Have an ACRP certification
  • Be bilingual in Spanish
  • Ability to effectively manage time and prioritize workload.
  • The ability to prepare and monitor budgets.

20. BS in Pathology with 1 year of Experience

  • Knowledge of Good Clinical Practices (GCP) and other Regulations
  • Must be detail-oriented, organized, and able to multitask in a fast-paced environment
  • Excellent communication, interpersonal and facilitation skills
  • Ability to work collaboratively with other members of the clinical research team and other sites
  • Computer competence, including proficiency in Microsoft Word, Excel, and PowerPoint
  • Keen knowledge of data management programs.
  • Ability to prioritize tasks and set deadlines.

21. BS in Clinical Laboratory Science with 3 years of Experience

  • Clinical skills, including the ability to perform phlebotomy
  • Clinical research coordinator experience
  • Excellent communication and organizational skills
  • Must be detail-oriented
  • Familiarity with the Code of Federal Regulations as they pertain to human subject protection
  • Strong interpersonal skills
  • Strong computer skills, Internet applications and Microsoft Office Suite
  • Nursing licensure, Medical assistant, or EMT certifications

22. BS in Biotechnology with 2 years of Experience

  • A strong background in the biological sciences, medicine or public health
  • Excellent oral and written communication skills
  • Experience with managing clinical data in a research setting
  • Proficiency in using computers, software, and web-based applications in a previous administrative setting
  • Experience training, mentoring, and/or supervising others on topics related to clinical research conduct and management
  • Proficiency in Spanish (verbal and written)
  • Ability to identify problems and develop sound solutions.

23. BS in Health and Human Services with 3 years of Experience

  • Background in a health-related field, especially exercise science, exercise physiology, or physical therapy.
  • Strong working knowledge of fitness and exercise principles and training guidelines.
  • Prior clinical research experience and institutional review board process.
  • Previous study coordination experience.
  • Ability to operate a personal computer and various software packages such as Word, EXCEL, and PowerPoint.
  • Attention to detail with excellent time management skills
  • Strong work ethic, self-motivated, and willing to learn
  • Good interpersonal and organizational skills with excellent written and verbal communication skills
  • Ability to work in a multi-disciplinary team setting as well as independently.

24. BS in Biotechnology with 2 years of Experience

  • Related working experience.
  • Demonstrated high-level communication skills to convey information in a clear and concise way, synthesizing information and presenting it to others.
  • Strong and proven organization and administrative skills - scheduling, data/file management, word processing (Microsoft Word), spreadsheets (EXCEL), copying, phone skills, data entry.
  • Willingness to work as a supportive, cooperative member of an interdisciplinary team.
  • Demonstrated problem-solving capabilities to resolve concerns that arise unexpectedly.
  • Ability to research, properly evaluate information, and prepare concise, well-organized reports, summaries, and correspondence.
  • Demonstrated ability to organize and prioritize a complex and dynamic workload.
  • Ability to multitask and meet deadlines, despite interruptions.
  • Ability to independently exercise discretion and sound judgment.
  • Ability to work collegially and cooperatively in a small office and to establish and maintain cooperative working relationships.

25. BS in Epidemiology with 1 year of Experience

  • Working experience in a similar role
  • Knowledge of venepuncture/cannulation would be an added advantage
  • Good time management and communication skills
  • Able to work independently
  • Must have computer literacy
  • Ability to work within a deadline-driven structure.
  • High level of integrity and honesty in maintaining confidentiality.
  • Foster and promote a positive attitude and professional appearance.

26. BS in Neuroscience with 6 years of Experience

  • Fluency in the usage of the Committee of Human Research (CHR) online iMEDris system for submission, renewal, and modification of protocols through this system
  • Understanding of the patient population to create rapport and a relationship, while also giving insight into what is realistic and appropriate for patient participation
  • Experience with electronic medical records
  • Knowledge of UCSF and departmental policies for dealing with reimbursement, guidelines for research, confidentiality, and HIPAA regulations, following the UCSF mission statement and purpose for research
  • A clear understanding of policies and procedures on patient safety and confidentiality (electronic and hard copy medical records, patient charts, communication, etc)
  • Knowledge of medical terminology, research policies and guidelines, and guidelines for packing/shipping infectious substances
  • Knowledge of database building/analysis, and data management within some of Access, Stata, SASS/SPSS, and Teleform programming platforms
  • Familiarity with nephrology research
  • Experience applying the following regulations and guidelines
  • Attention to detail, strong interpersonal and communication skills to coordinate with subjects, team members, other departments, and outside institutions
  • The ability to multitask in a fast-paced environment while working with a diverse subject population
  • Ability to work well independently, complete projects on time, and prioritize multiple projects to ensure the completion of essential tasks by deadlines

27. BS in Medical Laboratory Science with 3 years of Experience

  • Proven ability to lead a research team in the execution of trials within the scope of the established study protocol.
  • Demonstrated skill in meticulous attention to study requirements, regulatory constraints, and accurate follow-through.
  • Ability to prepare and submit regulatory documents and maintenance requirements for the life of the trials
  • Thoroughly skilled in obtaining informed consent and related research subject interactions and requirements.
  • Proven ability to track multiple occurrences and outcomes and document the same promptly.
  • Exceptional organizational skills.
  • Demonstrated independence and management skills among multiple study sites.
  • Demonstrated ownership of communication requirements necessary for effective oversight and conduct of human clinical research utilizing multiple electronic data capture systems.

28. BS in Biochemistry with 4 years of Experience

  • Experience with clinical research trials.
  • Experience in patient privacy laws and regulatory IRB submissions.
  • Experience performing clinical research duties in a clinical research environment and remotely.
  • Experience using statistical software applications.
  • Knowledge of database, word processing, and spreadsheet applications such as CREDIT, Access, Excel and MS Word.
  • Experience with laboratory procedures and values, and experience in interpreting them to determine patient eligibility and potential toxicities.
  • Ability to maintain confidentiality.
  • Excellent communication skills, both oral and written, using grammatically correct English. 
  • Excellent interpersonal skills, including tact, diplomacy, and flexibility. 
  • Demonstrated ability to interact effectively with diverse groups, including professional and non-professional staff and clients.

29. BS in Health Information Management with 3 years of Experience

  • Experience as a clinical research coordinator 
  • Must have experience with late-phase drug and device trials (phase 2, 3, 4).
  • Certified Clinical Research Coordinator (SOCRA or ACRP)
  • Ability to manage multiple projects, meet deadlines, and adjust priorities appropriately in an evolving work environment with shifting time frames
  • Self-starter with a high degree of initiative, urgency, and follow-through.
  • Commitment to and role model of the company's values with the ability to demonstrate those positively and proactively to patients, teammates, management, physicians, and/or vendors (Village Service Partners) in everyday performance and interactions
  • Travel up to 10%, depending on business needs.
  • Experience in managing confidential information and/or issues using discretion and judgment.

30. BS in Genetics with 4 years of Experience

  • Professional certifications such as the CCRP, CCRC, CIRB, or CRA
  • Previous research experience and must do a test.
  • Experience in a research role requiring the use of laboratory protocol, systems, and documentation techniques
  • Detailed knowledge of human subject research regulations
  • Strong demonstrated attention to detail and ability to adhere to policies and procedures.
  • Excellent verbal and written communication skills and interpersonal skills
  • Must be familiar with Word, PowerPoint, and Excel.
  • Knowledge of FDA and or EMEA Regulations, ICH Guidelines, GCPs, and familiarity with standard clinical operating procedures
  • Ability to analyze problems, implement solutions, and multitask.
  • Demonstrated experience in maintaining flexibility and adaptability while implementing institutional change.

31. BS in Medical Laboratory Science with 1 year of Experience

  • Working knowledge of medical/dental terminology.
  • Innovative thinker with strong conceptual and problem-solving skills.
  • Meticulous attention to detail with the ability to multitask.
  • Strong organizational, administrative, and planning skills.
  • Ability to work in high-pressure situations.
  • Ability to work independently and as part of a team.
  • Excellent documentation, communication, and computer skills.

32. BS in Biotechnology with 2 years of Experience

  • Experience working in clinical research coordination
  • Ability to converse in mainstream languages (able to speak in local dialects) to handle patient queries on the research study
  • Strong organizational skills, able to work independently
  • 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.

33. BS in Toxicology with 1 year of Experience

  • Knowledge of the pharmaceutical/healthcare industry
  • Excellent customer service and people skills
  • Ability to work independently as well as within teams
  • Attention to detail and the ability to prioritize
  • Strong organizational skills
  • Proficient in MS Word, PowerPoint, Outlook, Excel, etc.
  • Ability to take initiative and demonstrate strong commitment to duties.

34. BS in Health Informatics with 2 years of Experience

  • Registered with the Singapore Nursing Board (SNB).
  • Clinical research and nursing experience
  • Meticulous, possesses good interpersonal and organisational skills.
  • Able to work independently as well as in a team
  • Possesses professional knowledge of a wide range of nursing concepts, principles, and practices
  • Trained in Venipuncture and Cannulation
  • Demonstrated skill in interacting with persons of various social, cultural, economic, and educational backgrounds.
  • Ability to think critically, compile data from various sources, analyze data, and prepare reports.

35. BS in Environmental Health with 3 years of Experience

  • Experience working as a CRC
  • Ability to check and document vitals as well as EKG (ECG)
  • Experience working in Phlebotomy
  • Good management and organizational skills
  • Understanding of medical procedures
  • Exceptional interpersonal skills, the ability to work independently
  • The ability to lift a minimum of 50 pounds
  • Command of professional and Business English (written and spoken)
  • Skill in working independently, taking initiative, and following through on assignments.

36. BS in Behavioral Science with 5 years of Experience

  • Hands-on experience in Patient Care
  • Recent clinical research experience
  • Computer literate (EMRs, Microsoft Office applications, etc.)
  • Recent phlebotomy, specimen collection, processing, and shipping.
  • Provide a high level of quality patient care and customer service at all times
  • The ability to plan, prioritize, and complete multiple tasks
  • Work well under pressure, assess, respond to, and communicate issues promptly
  • Must maintain composure and set a professional example for patients and coworkers
  • Communicate clearly with patients and coworkers through the telephone, email, and in person
  • The ability to interpret and apply clinical and non-clinical policies and procedures
  • Be reliable, punctual, and able to work independently and with flexibility to accommodate protocol requirements

37. BS in Health Informatics with 2 years of Experience

  • Experience in a clinical or lab setting, including coursework.
  • Previous experience as a research coordinator
  • Certified Ophthalmic Associate or Certified Ophthalmic Technician certifications
  • Medical skills and/or certifications such as (CPT) certified phlebotomist technician, (EMT) Emergency Medical Technician
  • Ability to work both independently and as part of a team.
  • A team player with a strong interest in clinical studies, and enjoys interacting with patients
  • Strong attention to detail.
  • The ability to work a flexible schedule, including weekends

38. BS in Genetics with 4 years of Experience

  • Experience in an R&D Department or Clinical Research, including experience managing the execution of a study or trial protocol as a project manager of the study/trial or clinical study/trial coordinator
  • State license and certification in phlebotomy, CPR, AED, and adult first aid
  • Current certification with clinical research under CITI (GCPs, HIPAA)
  • Certification in Clinical Research (such as ACRP or SOCRA Certification for CRA or CRC)
  • A strong communicator and collaborator, and works effectively with all members of the organization, from individual contributors to top execs
  • Strong written and oral communication skills
  • Good time management and the ability to prioritize tasks and efficiently accomplish goals
  • Knowledge of laboratory certification processes and standards
  • Excellent attention to detail and ability to maintain detailed and accurate records
  • Highly analytical and strategic with solid problem-solving skills
  • Willing to always maintain a friendly disposition, even (and especially) under pressure

39. BS in Pre-Medicine with 1 year of Experience

  • Experience as a Clinical Research Coordinator, preferably with practice coordinating industry-sponsored trials in a private setting.
  • Be an energetic, go-getter who is detail-oriented and can multitask.
  • Be goals-driven while continuously maintaining quality.
  • Have an ACRP certification
  • Have vaccine working experience
  • Experience with computer systems, including web-based applications and Microsoft Office applications - Outlook, Word, Excel, PowerPoint, or Access.

40. BS in Medical Laboratory Science with 2 years of Experience

  • Experience in a medical setting and/or clinical research
  • Current Clinical Research Coordinator (CRC) Certification by ACRP, SOCRA, or equivalent, including ACRP-CP
  • Excellent written and verbal communication skills
  • Strong organizational skills with attention to detail and accuracy
  • High proficiency level in Microsoft Outlook, Word, Excel, and PowerPoint
  • Superior interpersonal skills
  • Self-starter who is personally accountable to prioritize and complete tasks to deliver desired outcomes within allotted time frames.

41. BS in Public Health with 3 years of Experience

  • Clinical research experience as a clinical research coordinator or similar position.
  • RN or vocational education in a health care-related discipline.
  • Hold a CCRC certification
  • Must be proficient in clinical procedures such as phlebotomy, vital signs, and ECGs.
  • Knowledge and understanding of general medical terminology, clinical methods, procedures, and applications.
  • Knowledge and understanding of the principles of good clinical practices, including ethical issues, patient rights, regulations, and guidelines for clinical research.
  • Excellent written and verbal communication skills.
  • Extensive working knowledge of GCP, ICH, and other research industry norms.
  • Team building and leadership skills with strong problem-solving ability
  • Customer service, strong interpersonal skills, with the ability to improve processes.

42. BS in Clinical Research with 1 year of Experience

  • Related work experience
  • Proficiency with the Microsoft Office Suite
  • Excellent verbal and written communication skills
  • Ability to work independently and collaboratively, in a fast-paced, matrixed team environment consisting of internal and external team members
  • Analytical thinker with excellent problem-solving skills
  • The ability to adapt to changing priorities and deadlines
  • Excellent planning, organization, and time management skills, including the ability to support and prioritize multiple projects

43. BS in Health Sciences with 3 years of Experience

  • Related work experience in a similar job family. 
  • Experience indicating ability to work with minimal supervision in a team atmosphere and receptiveness to direction regardless of disease area. 
  • Ability and skill for laboratory processing, phlebotomy, and vital sign execution. 
  • EKG (electrocardiogram or ECG) capabilities
  • Clinical Coordinator Certification (SoCRA or equivalent).
  • Strong interpersonal skills with the ability to effectively interact with all levels of staff and external contacts.
  • Must be detail-oriented and have the ability to follow through.
  • Advanced Microsoft Office Word, Excel, and PowerPoint

44. BS in Biomedical Sciences with 7 years of Experience

  • Prior experience as a Research Coordinator.
  • Familiarity with critically ill adult and/or pediatric populations and/or experience in burn surgery research
  • Advanced level knowledge and understanding of federal, state, and university (or similar) regulations for clinical research under Investigational New Drug and Institutional Review Board (IRB) guidelines (or similar).
  • Experience in independently comprehending and implementing complex clinical research protocols, with careful attention and strict adherence to detail.
  • Experience coordinating a broad range of activities from inception to implementation within the confines of strict study protocols, a University (or similar), and policies and procedures.
  • Expertise using analytical and problem-solving skills for the identification and resolution of unique and unforeseen problems in a logical, timely, and often creative manner 
  • Expertise in maintaining the integrity of study protocols and legalities defined by the University (or similar) policies and procedures.
  • Advanced-level skills in preparing correspondence, recruitment materials, manuscripts, contracts, and budgets.
  • Excellent and advanced knowledge of grammar, punctuation, and syntax for editing and proofing to produce error-free work.
  • Excellent skills to communicate in writing using clear, expository prose.
  • Excellent listening skills and intermediate to advanced level skills to translate into a coherent written synopsis.
  • Advanced level understanding of the organizational culture of an academic/medical department in a large public university (or similar).
  • Knowledge of personnel, travel, accounting, and University policies, procedures, and systems.
  • College-level knowledge of human anatomy and medical terminology.

45. BS in Health Sciences with 6 years of Experience

  • Experience in independently organizing tasks and setting priorities for work assignments to achieve timely progress on multiple tasks simultaneously
  • Thorough knowledge and understanding of “Good Clinical Practices” for clinical research.
  • Excellent skills to exercise discretion, initiative, and resourcefulness and make independent judgments based on sound analysis.
  • Advanced-level organizational skills and attention to detail in maintaining large volumes of records.
  • Administrative skills and ability to exercise judgment, initiative and resourcefulness in making decisions.
  • Excellent oral and written communication skills
  • Knowledge of anatomy, physiology, medical terminology, and procedures to effectively interpret and accurately compile data according to study protocol.
  • Excellent mathematical calculation to perform basic accounting skills, calculate testing equations and perform statistical calculations.
  • Advanced-level computer skills for word-processing programs, database programs, and data management.
  • Excellent writing and printing skills to document research data onto forms and to prepare other IRB (or similar) documentation.
  • Excellent interpersonal skills to communicate in a courteous, professional, effective and informative manner in person and on the telephone with a wide variety of people.
  • Excellent skills in maintaining good working relationships with faculty, community-based healthcare professionals, staff and research participants.
  • Experience exercising integrity and discretion in all matters and to protect confidential information and/or protected health information as dictated by assignment, policy or regulation.

46. BS in Neuroscience with 3 years of Experience

  • Experience working as a Clinical Research Coordinator
  • Experience working in neurology research
  • Previous nursing work experience
  • Knowledge of federal regulations, good clinical practices (GCP)
  • Knowledge of medical and research terminology
  • Computer skills including use of clinical trial database, electronic data capture, and MS Word or Excel
  • Excellent communication and interpersonal skills
  • The ability to communicate and work effectively with a diverse team of professionals
  • Organizational and prioritizing capabilities
  • The ability to work independently in a fast-paced environment with minimal supervision at off-site facilities

47. BS in Health and Human Services with 6 years of Experience

  • Current Basic Life Support (BLS) certification from the American Heart Association
  • Relevant research experience in a clinical setting.
  • Experience working independently, organizing work, and setting priorities.
  • Experience In the area of assigned clinical specialty
  • Experience in clinical research
  • Experience with data entry and database management
  • Effective verbal and written communication skills and the ability to present information clearly and professionally to varying levels of individuals throughout the patient care process.
  • Must have computer skills and dexterity for data entry and retrieval of information
  • Must be proficient with Windows-style applications, various software packages specific to the role, and keyboard shortcuts
  • Critical thinking skills to apply to the process of trial evaluation and submission, particularly the development of study-related budgets, contracts and patient consent documents

48. BS in Healthcare Administration with 5 years of Experience

  • Experience as a Research Coordinator I or performing the role of a Research Coordinator I
  • Proficiency with a variety of computer-based skills, especially in the use of word processing, spreadsheets, databases, and presentation software, and the ability to undertake internet searches.
  • Solid written and verbal communication skills.
  • Must be self-directed with demonstrated ability to work in collaboration and cooperation with members of a multidisciplinary team.
  • Within 90 days of hire, must complete certification in Human Subjects Research as required by the Responsible Conduct of Research guidelines adopted by the Cleveland Clinic.
  • Independent thinking skills, decisive judgment, and the ability to work with minimal supervision.
  • Must be able to work in a stressful environment and take appropriate action.
  • A high degree of dexterity to produce materials on a computer.
  • Normal or corrected vision and hearing within the normal range.
  • Extensive sitting and frequent walking, occasional lifting or carrying up to 25 pounds.
  • Have some exposure to communicable diseases or body fluids.

49. BS in Epidemiology with 7 years of Experience

  • Experience with post-activation coordination of research studies and managing approximately 6 protocols.
  • Prior experience with data abstraction and data entry.
  • Experience coordinating and monitoring clinical trials related specifically to Oncology and/or neurosurgery, either in industry or at UCSF.
  • Experience working with oncology or neurosurgical patients.
  • Prior experience working in a medical setting, either office or a hospital.
  • UCSF Clinical research experience.
  • Experience with electronic IRB submissions (iMedRIS).
  • Experience with UCSF Cancer Center (OnCore) patient tracking and data entry.
  • Completion of UCSF Clinical Research Study Coordinator training.
  • Previous experience, or willingness, to perform neurocognitive assessments or other direct patient interactive, non-therapeutic tasks related to the needs of the clinic and specific clinical trials as assigned, or that come up during the clinic
  • Experience working in clinical research
  • Experience applying the following regulations and guidelines as it relates to clinical trials in Oncology - Good Clinical Practice Guidelines, Health Information and Accountability Act (HIPAA), The Protection of Human Research Subjects, CHR regulations for recruitment and consent of research subjects, Effective Cash Handling Procedures, Environmental Health and Safety Training, Fire Safety Training
  • Ability to work well independently, complete projects on time, and prioritize multiple projects to ensure the completion of essential tasks by deadlines

50. BS in Allied Health with 5 years of Experience

  • Experience working as an Assistant CRC.
  • Ability to work professionally and as part of a team with experience supervising a team, reporting progress, and problem-solving.
  • Strong ability to multi-task, prioritize, and follow up to keep track of ongoing or new problems and requests.
  • Skill in writing concise and understandable documentation of procedures.
  • Proficient writing skills to prepare and review a variety of materials with accuracy and completeness.
  • Ability to communicate effectively both verbally and in writing with study participants, researchers, and non-researchers.
  • Excellent interpersonal skills to relate easily and effectively with people within and outside the University, including both strong written and verbal communications.
  • Ability to work with online calendars, databases, and tracking tools.
  • Skill to use a personal computer, computer software programs at the level of sophistication for general office work, and knowledge of Outlook, Word, Excel, and PowerPoint.
  • Familiarity with the Internet and how to conduct searches.
  • Familiarity with the Health Insurance Portability and Accountability Act of 1996 (HIPAA) to ensure confidentiality, privacy, and security of patient information.

51. BS in Psychology with 6 years of Experience

  • A background in pre-med, psychology, neuroscience, or a related field
  • Previous experience in a research setting with experience interacting with human research participants
  • Experience working in an office and a clinic environment
  • Ability to work well with minimal supervision, prioritizing work according to and within established study protocols
  • Excellent organizational skills to accomplish a variety of responsibilities and to establish and maintain efficient systems.
  • Excellent interpersonal skills to be able to interact with a variety of people in person and on the telephone.
  • Must be able to relate well with subjects, physicians, technologists and administrators.
  • Ability to work under stress and within deadlines (the clinical research setting is a very busy and demanding environment)
  • Experience with word processing software, with Microsoft Excel experience
  • English/Spanish bilingual
  • Must be able to travel between the hospital and research buildings carrying study documents and materials.

52. BS in Biotechnology with 2 years of Experience

  • Related working experience with knowledge of medical terminology.
  • Society of Clinical Research Associates or Association of Clinical Research Professionals certification
  • Effective oral, written communication, interpersonal skills.
  • Must be able to work under the direction of supervision.
  • Ability to identify, analyze, and solve problems.
  • Time management skills and the ability to work well under pressure.
  • Proficiency in using various Microsoft Office applications such as Word, Excel, Access, PowerPoint, and Outlook.
  • Familiar with Internet applications.

53. BS in Public Health with 1 year of Experience

  • An interest in psychology, medicine, health behaviors, public/community health, or a related field
  • Superior organizational, administrative, and time management skills
  • Strong computer skills, experience working with databases, spreadsheets, and word processing programs, and ability to use Microsoft Office (Access, Excel, Word, PowerPoint)
  • The ability to interact professionally with office staff as well as with vulnerable research participants
  • Excellent English language skills (grammar and spelling), with good telephone and in-person communication skills
  • Intellectual independence and initiative
  • A self-starter who works well as a member of a team yet has ambition and drive to take on tasks independently.
  • Must be able to handle and prioritize multiple tasks, have strong organization skills, and pay close attention to detail

54. BS in Medical Laboratory Science with 3 years of Experience

  • Experience working in clinical research
  • Ability to work fast and efficiently within time constraints
  • Ability to work independently and comfortably with study participants
  • Prior data entry and management experience
  • General knowledge of medical terminology.
  • Ability to work with human study participants as well as in a team
  • Attention to detail in data collection and excellent organizational skills
  • Ability to work under deadlines with general guidance
  • Strong written and oral communication skills
  • General computer skills and ability to quickly learn and master computer programs such as REDCap, Microsoft Office
  • Ability to interpret, adapt, and apply guidelines and procedures

55. BS in Psychology with 4 years of Experience

  • Previous research experience, preferably experience in child development, neuropsychology, or related fields
  • Experience working or interacting with children and adolescents
  • Ability to work independently, take initiative, and problem-solve effectively
  • Strong organizational skills and attention to detail
  • Strong interpersonal and communication skills
  • The ability to work collaboratively with research participants, supervisors, coworkers, and student supervisees
  • Familiarity with basic statistical and data management software (e.g., SPSS, REDCap)
  • Skill in completing assignments accurately and with attention to detail.
  • Ability to analyze, organize, and prioritize work under pressure while meeting deadlines.
  • Ability to work evenings, nights, and weekends

56. BS in Neuroscience with 3 years of Experience

  • Work-related experience in Clinical Research, ideally within the field of neurology/neuroscience, with patient interaction/evaluation.
  • Experience with the regulatory aspects of clinical research
  • Ability to work independently and collaborate with a team.
  • Excellent verbal and written communication skills
  • 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.

57. BS in Pre-Medicine with 2 years of Experience

  • A background in pre-med/neuroscience with prior lab experience
  • Directly related work experience will be considered for a Clinical Research Coordinator II position.
  • Must have very strong written and verbal communication skills
  • Must be driven to work productively under minimal supervision
  • Proficient with computers and databases, and able to troubleshoot and problem-solve independently
  • Capable of being friendly and communicative with labmates and study participants, and assertive when confronted with obstacles
  • Respectful of study participants' rights and individual needs
  • Experience with Linux, coding, or neuroimaging

58. BS in Pharmacology with 1 year of Experience

  • Experience working in a medical or scientific research setting or a comparable technology-oriented business environment
  • Excellent organization and communication skills
  • Strong interpersonal skills, ability to effectively interact with all levels of staff and external contacts.
  • Must be detail-oriented and have the ability to follow through.
  • Ability to effectively manage time and prioritize workload.
  • Must practice discretion and adhere to hospital confidentiality guidelines at all times.
  • Must have computer skills, including the use of Microsoft Office.

59. BS in Biomedical Sciences with 3 years of Experience

  • Experience in a medical setting and/or clinical research
  • Experience with computer systems, including web-based applications and Microsoft Office applications - Outlook, Word, Excel, PowerPoint or Access.
  • Ability to make decisions that are guided by general instructions and practices requiring some interpretation, and make recommendations for solving problems of moderate complexity and importance.
  • Ability to address varied problems, requiring analysis or interpretation of the situation using direct observation, knowledge, and skills based on general precedents.
  • Ability to follow precedents and procedures, set priorities and organize work within general guidelines.
  • Ability to communicate clearly and effectively in written English with internal and external customers.
  • Ability to comprehend and converse in English to communicate effectively with medical center staff, patients, families and external customers.
  • Ability to demonstrate full working knowledge of standard concepts, practices, procedures and policies with the ability to use them in varied situations.
  • Ability to work collaboratively in small teams to improve the operations of the immediate work group by offering ideas, identifying issues, and respecting team members.
  • Ability to demonstrate a positive attitude and respond to requests in a timely and respectful manner.

60. BS in Physiology with 5 years of Experience

  • Experience in the field or a related area.
  • Strong attention to detail and customer service focus
  • Excellent communication, organizational, presentation, documentation, and interpersonal skills
  • The ability to work independently or in a team and handle multiple deadline-driven tasks in a dynamic environment
  • Proficiency in Microsoft Office Suite (Word, Excel, and PowerPoint), email (Outlook), and voicemail
  • Able to review and comply with all relevant HUMC and Business Unit policies and procedures, and local, state, and Federal laws and regulations.
  • Mandatory education on human subject research and GCP (CITI Training and Certification).
  • Knowledge of clinical trials and the regulation (local, state, and federal) of such.
  • Familiarity with basic scientific and healthcare principles and terminology.
  • Ability to work in a fast-paced environment and manage competing tasks and demands.

61. BS in Biotechnology with 2 years of Experience

  • Knowledge of medical terminology/environment.
  • Ability to interact and communicate with clarity, tact, and courtesy with patrons, patients, staff, faculty, students, and others.
  • Ability to communicate with tact and diplomacy.
  • Strong organizational and communication skills (verbal and written).
  • Excellent interpersonal skills.
  • Strong data management skills and attention to detail.
  • Knowledge of Microsoft Word, Excel, and Adobe Acrobat.
  • Ability to read and understand complex documents (e.g., clinical trials).
  • Ability to handle competing demands with diplomacy and enthusiasm.
  • Ability to absorb large amounts of information quickly.
  • Adaptability to changing working situations and work assignments.

62. BS in Neuroscience with 1 year of Experience

  • Experience in clinical research, preferably nephrology experience
  • Basic knowledge of FDA regulations, IRB requirements, and Good Clinical Practice.
  • Basic knowledge of kidney care and/or End-Stage Kidney Disease (ESKD) or a similar field
  • Strong verbal and written communication skills
  • Must have intermediate computer skills, including Microsoft Office (Word, Excel, Outlook, and web-based tools)
  • Proficiency in USRC applications
  • Ability to process and handle confidential information with discretion.
  • Ability to work independently and/or in a collaborative environment.

63. BS in Healthcare Administration with 2 years of Experience

  • Experience working in women’s health
  • Strong communication and interpersonal skills.
  • Proficiency with Microsoft Office.
  • Knowledge of medical terminology
  • Demonstrates the ability to work well with colleagues and clients and with external organizations.
  • Demonstrates commitment to personal responsibility and value for safety, and communicates safety concerns
  • Must use and promote safe behaviors based on training and lessons learned.
  • Ability to analyze, organize, and prioritize work under pressure while meeting deadlines.
  • Skill in completing assignments accurately and with attention to detail.

64. BS in Biology with 4 years of Experience

  • Background in neuropsychology, neuroscience, biology, bioengineering, or a related field with research experience
  • Experience working with individuals with psychotic disorders and children/adolescents
  • Availability for flexible scheduling, including evenings and weekends.
  • Strong organizational, leadership, supervision, communication, and computer skills.
  • Must pass Pennsylvania’s Child Protective Services Act (also known as Act 73) background checks, within 30-90 days of employment.
  • Experience conducting MRI research in a research-oriented facility
  • Experience operating an MRI Console (e.g., Protocol selection and scan parameter set-up, MR system RF coils, table operation, patient positioning)
  • Strong computer and technical skills
  • Excellent interpersonal and communication skills
  • Excellent troubleshooting and problem-solving skills

65. BS in Radiologic Technology with 3 years of Experience

  • Previous clinical research experience
  • Previous experience in oncology research
  • CCRP or CCRC accreditation
  • Must be able to work independently and with multidisciplinary teams, and interact with participants
  • Be self-motivated, able to multitask, prioritize, and problem solve
  • Exceptional interpersonal skills both in-person and on telephone calls
  • Must be a self-starter with the ability to locate resources and operate productively in an environment where standard operating procedures, guidelines, and policies are not always available
  • Collaborative focus, as well as strong written and verbal communication skills, including computer skills

66. BS in Pathology with 1 year of Experience

  • Prior clinical research experience
  • Enjoy interaction with people, including infants
  • Ability to work both independently and in a team
  • Possesses excellent communication and interpersonal skills
  • Self-motivator, proactive, meticulous, and possesses excellent organizational skills
  • Multi-tasking capabilities
  • Must have strong Microsoft Office skills
  • Able to work flexibly with occasional weekends and late nights when required by the project.

67. BS in Nursing with 2 years of Experience

  • Experience in hands-on clinical trials coordination
  • Experience in nursing, science, or research
  • Strong computer literacy with knowledge of clinical trials software and the MS Office suite
  • Excellent communication and interpersonal skills with the ability to work both independently and as part of a team in an effective, pro-active and co-operative manner
  • High level of initiative and flexibility, and the ability to meet deadlines while balancing multiple priorities
  • Knowledge of Good Clinical Practice and applicable national and international laws and regulations.
  • Flexibility in working times and locations
  • The ability to travel interstate

68. BS in Biomedical Sciences with 3 years of Experience

  • Knowledge of medical and research terminology
  • Knowledge of the FDA Code of Federal Regulations and GCP
  • Knowledge of the clinical research processes
  • Strong public presentation skills
  • The ability to manage multiple ongoing priorities and projects with a diverse team of professionals
  • Oncology experience, preferably in hematology/oncology and/or transplant
  • Experience in a clinical research setting
  • Experience managing blood cancer and/or BMT clinical trials
  • Research certification (ACRP or CCRP), RN or LPN

69. BS in Physiology with 5 years of Experience

  • Experience in oncology clinical research
  • Professional certification (ACRP CCRC or SOCRA CCRP), CITI GCP and C-14 certifications
  • Prior experience with laboratory information management systems (LIMS)
  • Good interpersonal, writing, and verbal communication skills. 
  • Clinical research experience or related research laboratory experience. 
  • Must be able to work under the direction of supervision. 
  • Ability to identify, analyze, and solve problems. 
  • Time management skills and the ability to work well under pressure. 
  • Proficiency in using various Microsoft Office applications such as Word, Excel, Access, PowerPoint and Outlook. 
  • Familiar with Internet applications. 
  • Intermediate competency in medical terminology, and an advanced competency in Good Clinical Practice (GCP) guidelines, Federal Regulations that govern the conduct of human subjects research, as well as Institutional Review Board and institutional policies and procedures related to human subjects research.

70. BS in Medical Laboratory Science with 3 years of Experience

  • Experience as a Clinical Research Coordinator 
  • Monitoring experience in a clinical research environment and administrative Institutional Review Board (IRB) experience.
  • Knowledge of human and animal subject research regulations and federal guidance documents
  • Current certification as a Certified Clinical Trial Investigator (CCTI), Certified Clinical Research Coordinator (CCRC), or Certified Clinical Research Professional (CCRP) from the Association of Clinical Research Professionals (ACRP) or the Society of Clinical Research Associates (SoCRA)
  • Prior experience with a medical agency
  • Competent in the use of data analysis tools (e.g., MS Excel and MS Access) and statistical tools (e.g., SPSS)
  • Strong communication and writing skills
  • Must be a strong team player
  • Able to analyse data and conduct literature reviews

71. BS in Pharmacology with 2 years of Experience

  • Previous experience with therapeutic clinical research involving drugs and/or devices.
  • Experience in Phase I, II, and III clinical research.
  • Experience navigating medical records and data extraction.
  • SOCRA/ACRP Certification.
  • Study coordinator experience or experience in oncology clinical trials
  • Oncology study coordinator experience.
  • Exceptional interpersonal skills, the ability to work independently
  • Command of professional and Business English (written and spoken)

72. BS in Biochemistry with 4 years of Experience

  • Relevant work experience in a clinical environment or medical setting, e.g., medical assistant, assistant nurse, laboratory technician
  • Working knowledge of clinical trials
  • Working knowledge of the principles of Good Clinical Practices (GCP)
  • In-depth knowledge of departmental, protocol, and study-specific operating procedures, consent forms, and study schedules
  • Skill in carrying out clinical procedures such as intravenous catheter insertion and spirometry testing
  • Good skill in using MS Windows and Office applications such as Access, Outlook, and Word
  • Excellent interpersonal skills
  • Ability to pay close attention to detail
  • Ability to establish and maintain effective working relationships with coworkers, managers, and clients

73. BS in Health Information Management with 3 years of Experience

  • Relevant research work experience
  • Experience with research protocols and regulatory or governing bodies, including HIPAA and FDA regulations, Institutional Review Board requirements, and Good Clinical Practices.
  • Knowledge of medical terminology.
  • Strong interpersonal and communication skills
  • Proficiency with Microsoft Office and database applications.
  • SOCRA/ACRP Certification or eligible for certification
  • Hold a BLS certification 
  • Ability to oversee complex projects with strict protocols, with strong attention to detail
  • The ability and willingness to travel

74. BS in Microbiology with 2 years of Experience

  • Experience working in clinical research
  • Health care Professional or Research training (Master’s level)
  • Fluent in French and English, spoken and written
  • Self-directed and organized, and able to work both independently and as part of a team
  • Excellent interpersonal skills
  • Strong proficiency in Microsoft Office programs (Word, Excel, PowerPoint) and Web applications
  • Ability to manage both patient and physician expectations
  • Good organizational skills with strong problem-solving ability

75. BS in Clinical Laboratory Science with 3 years of Experience

  • Experience in pediatric clinical research in a hospital setting
  • Previous research and working experience
  • Bilingual in English/Spanish
  • Clinical research certification (such as CCRC, CCRP, CRA) and IATA certification
  • Excellent communication skills in working with both children and adults.
  • Good organizational skills, detail-oriented, people-oriented, self-confident, flexible, and adaptable to change.
  • Strong time management skills.
  • Knowledge of protocols and their process.
  • Software applications experience includes word processing, scheduling and contact database, email, web browsing, hospital records, other database software, and office equipment.
  • Worked with relevant hospital equipment for each clinical trial project.

76. BS in Pathology with 1 year of Experience

  • Previous experience with study coordination or in healthcare settings
  • Careful attention to details
  • Good organizational and communication skills
  • Ability to follow directions
  • Must have computer literacy
  • Working knowledge of clinical research protocols
  • Ability to demonstrate respect and professionalism for subjects’ rights and individual needs
  • Able to work in a fast-paced environment and have good time management skills.

77. BS in Microbiology with 2 years of Experience

  • Knowledge of medical and clinical research terminology and processes.
  • Ability to follow the investigational plan in the execution of study visits.
  • Working knowledge of requirements and regulations associated with the conduct of clinical trials and other related research activities.
  • Proficiency in using computers, software, and web-based applications, including working knowledge of Epic.
  • Effective verbal and written communication skills and the ability to present information clearly and professionally to varying levels of individuals throughout the patient care process.
  • Organizational and time management skills, and the ability to multitask and pay close attention to detail.
  • Ability to travel throughout and between facilities and work a flexible work schedule.
  • Meticulous, efficient, a team player, and possesses good interpersonal skills.

78. BS in Clinical Research with 5 years of Experience

  • Experience in a clinical research setting with protocols and clinical trials.
  • Expertise in the fundamentals of clinical trials.
  • Experience in clinical data management, data management, database operations, and analysis.
  • Experience with IRB and FDA requirements.
  • Strong writing skills.
  • Certified Clinical Research Professional (CCRP) or LVNRN CertificationsTraining CPR Certification from American Heart Association, Certified in Good Clinical Practices, Training in Human Subjects Protection (HSP)
  • A good decision-maker with proven success at making timely decisions that keep the organization moving forward.
  • Able to hold yourself and others accountable to achieve goals and live up to commitments.
  • An effective communicator, capable of determining how best to reach different audiences and executing communications based on that understanding.
  • Willing to take action and eager to embrace new opportunities and tough challenges with a sense of urgency, high energy, and enthusiasm.
  • Resilient in recovering from setbacks and skilled at finding detours around obstacles.

79. BS in Biomedical Sciences with 1 year of Experience

  • Passionate about medical terminology and science.
  • Experience working in a medical or scientific research setting
  • Excellent organization and communication skills
  • Strong interpersonal skills and the ability to effectively interact with all levels of staff and external contacts.
  • Must be detail-oriented and have the ability to follow through.
  • Ability to effectively manage time and prioritize workload.
  • Must practice discretion and adhere to hospital confidentiality guidelines at all times.
  • Must have computer skills, including the use of Microsoft Office

80. BS in Public Health with 3 years of Experience

  • Previous experience in clinical research or a health care-related field
  • Ability to obtain CRA/CRC certification on time.
  • Understanding of medical terminology and clinical research
  • Working knowledge of PCs and word processing, and data management software
  • Demonstrated analytical skills with accuracy and attention to detail.
  • Excellent verbal and written communication skills.
  • Goal-oriented and self-directive
  • Strong organizational and interpersonal skills.
  • Ability to actively participate as a team player.
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