MedTech Safety Project Lead
IQVIA · Washington, DC
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Role summary
IQVIA seeks a MedTech Safety Project Lead to provide operational and administrative support to the Clinical Safety team managing medical device and combination product safety activities. The role coordinates safety projects, independent safety review committees, documentation, and cross-functional collaboration across clinical and post-market programs.
Where this listing comes from
This listing was compiled by RoleLantern from the employer's publicly available posting on Workday, captured and rephrased by RoleLantern using automated (AI) tools on 2026-10-02 (originally posted 2026-10-02). It was not submitted or confirmed by the employer through RoleLantern. Details may be inaccurate, incomplete, outdated, or no longer available; please confirm with the employer's official posting before applying.
What they're looking for
- Bachelor's degree in Nursing, Life Sciences, Health Sciences, Public Health, Biology, or Biomedical Sciences
- Minimum 2 years of clinical, healthcare, clinical research, medical device, or patient care experience
- Strong organizational skills with ability to manage multiple priorities and deadlines
- Excellent verbal and written communication abilities
- Proficiency with Microsoft Office applications (Excel, Word, PowerPoint, Outlook)
- Demonstrated attention to detail and ability to maintain accurate documentation
- Ability to work effectively in collaborative, fast-paced environments
What you'll be doing
- Provide day-to-day operational and administrative support to the Clinical Safety team on medical device studies and post-market activities
- Serve as primary operational coordinator for assigned safety projects, ensuring deliverables, timelines, and documentation are executed successfully
- Assist with management of independent safety review committees including preparation of materials and documentation of outcomes
- Coordinate safety-related project tracking, timelines, documentation, meeting scheduling, and action item follow-up
- Support collection, review, and maintenance of safety documentation including adverse event reports and product complaints
Privacy & handoff
This role links to IQVIA's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.