Site Activation Manager (US)
Worldwide Clinical Trials · Durham, NC
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Site Activation Manager position at a global CRO responsible for managing study start-up activities, coordinating cross-functional teams, and ensuring timely completion of site activation projects. Reports to leadership and communicates project status to sponsors and internal stakeholders.
What they're looking for
- Four-year degree in medical, biological, health, pharmacy, or related science field
- Minimum four years CRO or pharmaceutical industry experience
- Experience in start-up management, project management, or site management
- Strong leadership and organizational planning skills
- Proficiency in cross-cultural and English communication
- Ability to manage independently and solve problems proactively
What you'll be doing
- Serve as primary point of contact for study start-up and site maintenance activities
- Oversee functional team activities to ensure critical path milestones meet timeline and budget targets
- Compile, manage, track and analyze site activation data and project metrics
- Support feasibility assessment and site identification as needed
- Communicate site activation and regulatory status updates to sponsors and project leadership
Compensation$86,000.00 - $170,000.00
Privacy & handoff
This role links to Worldwide Clinical Trials'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.