Sr. Clinical Project Manager
IQVIA · Washington, DC
Clinical OperationsFull-time$93k–$233kCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
IQVIA seeks a Senior Clinical Project Manager to oversee global MedTech clinical studies from planning through delivery. The role requires strategic leadership of multi-country programs, stakeholder management, and cross-functional team coordination to ensure regulatory compliance and successful outcomes.
What they're looking for
- Bachelor's degree in Life Sciences, Nursing, Biomedical Engineering, Public Health, or related scientific field
- Minimum 7 years clinical research experience with at least 4 years project management
- Experience managing clinical studies in MedTech, medical device, CRO, biotech, or pharma sectors
- Demonstrated leadership of global, multi-country clinical studies across multiple regions
- Strong knowledge of ICH-GCP, ISO 14155, FDA, and global regulatory requirements
- Proficiency with Microsoft Office and clinical trial management systems
- Proven ability to manage budgets, contracts, and cross-functional stakeholder relationships
What you'll be doing
- Lead planning, execution, and delivery of global MedTech clinical studies
- Serve as primary contact for sponsors and manage study timelines, budgets, and risk plans
- Oversee cross-functional teams to achieve milestones and ensure regulatory compliance
- Monitor study progress, identify project risks, and resolve issues proactively
- Mentor junior project management and clinical operations staff; drive process improvement initiatives
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.