Sr Site Activation Coordinator
IQVIA · Durham, NC
RoleLantern re-checked this role's application link recently and it was active — the employer has not confirmed it directly.
Role summary
IQVIA seeks a Senior Site Activation Coordinator to manage feasibility and site activation activities for clinical studies at the country/region level. The role involves preparing regulatory documentation, coordinating with internal teams and investigative sites, and maintaining project tracking systems in compliance with applicable regulations and SOPs.
What they're looking for
- Bachelor's degree in life science or related field
- 2 years of experience in healthcare environment or equivalent education and training
- Ability to review documents for completeness, consistency, and accuracy
- Proficiency with databases, tracking tools, and project management systems
- Strong organizational and communication skills for cross-functional coordination
What you'll be doing
- Perform site activation and feasibility activities for assigned clinical studies
- Prepare and review site regulatory, contractual, and ethics documents for accuracy
- Distribute completed documents to sites and internal project team members
- Update and maintain project databases, tracking tools, and timelines with current information
- Track progress and follow up on execution of regulatory documents, CDAs, ICFs, and Investigator Packs
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.