CLINICAL PROJECT LEAD SKILLS, EXPERIENCE, AND JOB REQUIREMENTS

Updated: Nov 21, 2024 - The Clinical Project Lead is well-versed in clinical laboratory workflows and research, with substantial experience in medical devices, drafting study protocols, SOPs, and generating reports. This role requires proficiency in a range of laboratory techniques, including Toxicology, Hematology, Chemistry, and Molecular, complemented by AMT or ASCP certifications. The lead also has effective project management and interpersonal skills to maintain relationships across diverse cultural backgrounds and deliver exceptional customer service.

Essential Hard and Soft Skills for a Standout Clinical Project Lead Resume
  • Clinical Trial Design
  • Regulatory Compliance
  • Data Analysis
  • Budget Management
  • Project Management Software
  • Clinical Protocol Development
  • Medical Writing
  • Statistical Software Proficiency
  • Risk Management
  • Pharmacovigilance
  • Leadership
  • Communication
  • Problem-Solving
  • Teamwork
  • Attention To Detail
  • Adaptability
  • Decision-Making
  • Conflict Resolution
  • Time Management
  • Empathy

Summary of Clinical Project Lead Knowledge and Qualifications on Resume

1. BA in Clinical Research Management with 6 years of Experience

  • Prior relevant experience in project management or equivalent combination of education, training and experience.
  • Advanced knowledge of the job area and broad knowledge of other related job areas.
  • Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i.e. ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial conduct. 
  • Broad protocol knowledge as well as therapeutic knowledge
  • Good understanding of the competitive environment and how to communicate/demonstrate value through IQVIA solutions.
  • Strong written and verbal communication skills including a good command of the English language
  • Strong presentation and problem-solving skills.
  • Ability to work through others to deliver results to the appropriate quality and timeline metrics, monitoring/managing performance and providing feedback.
  • Strong planning, time management and prioritization skills.
  • Attention to detail and accuracy in work. 

2. BA in Biomedical Sciences with 3 years of Experience

  • Previous working experience in a similar role.
  • Demonstrated project management skills (full project life cycle) with the ability to work on multiple projects simultaneously
  • Strong communication and presentation skills
  • Proficient in Microsoft Operating Systems
  • The willingness to travel
  • Knowledge of Digital photography
  • Must have excellent customer service skills.
  • Have American Medical Technologists (AMT) and/or the American Society for Clinical Pathology (ASCP) certifications.
  • Good understanding of project financials including experience managing, contractual obligations and implications.
  • Ability to demonstrate all IQVIA competencies (Client Focus, Collaboration, Communication, innovation, Ownership).

3. BA in Healthcare Administration with 5 years of Experience

  • Proven successful clinical research experience
  • Working experience in leading roles accountable for the planning, execution and reporting of global clinical trials of diverse development phases (I – IV)
  • Ability to lead cross-functional teams and to represent clinical operations in Core - Product Development Teams. 
  • Solid understanding of integrated development processes for pharmaceutical products.
  • Excellent leadership, project management, and resource management skills
  • Must have PMP certification
  • Extensive experience in financial oversight of a global clinical development program is desirable.
  • Line management working experience
  • Results-oriented approach to work towards delivery and output.
  • Good software and computer skills, including MS Office applications including Microsoft Word, Excel and PowerPoint.

4. BA in Public Health with 4 years of Experience

  • Clinical laboratory or clinical research experience, with medical device experience 
  • Must have experience drafting clinical study protocols, reports, SOPs
  • Demonstrated knowledge of clinical research/ clinical trial experience
  • Knowledge of laboratory workflow related to blood collection and handling
  • Have American Medical Technologists (AMT) and/or the American Society for Clinical Pathology (ASCP) certifications.
  • Project management working experience
  • Exposure to Toxicology, Hematology, Chemistry, Molecular, Flow Cytometry, or Coagulation Departments within the hospital setting
  • Experience working with IVD
  • The ability to establish and maintain effective working relationships with coworkers, managers and clients, understanding of cultural differences
  • Must have excellent customer service skills.
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