Sr. Site Activation Specialist (Medical device)
IQVIA · Shanghai, China +4 more
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
This role serves as the primary contact for assigned clinical trial sites, managing study activation, feasibility assessments, and regulatory documentation. The specialist coordinates between sites, project teams, and sponsors to ensure protocol adherence, timeline compliance, and quality deliverables throughout the activation process.
What they're looking for
- Bachelor's degree in life science or related field
- 3+ years clinical research experience
- 1+ year experience in leadership capacity
- Knowledge of clinical trial SOPs and regulatory requirements
- Proficiency with databases and project tracking systems
What you'll be doing
- Serve as primary contact between investigative sites, Site Activation Manager, and project teams
- Execute feasibility assessments, site identification, startup and activation activities
- Prepare and review site documents for completeness and regulatory compliance
- Track and monitor progress of regulatory, ethics, ICF and Investigator Pack documents
- Maintain internal systems and databases with accurate project-specific information
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.