Site Activation Manager
Worldwide Clinical Trials · Durham, NC
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Worldwide Clinical Trials seeks a Site Activation Manager in Durham, North Carolina to oversee site activation project management and delivery for assigned therapeutic areas. The role involves coordinating site identification, managing essential documents, monitoring contracts, and ensuring compliance with GCP and regulatory standards.
What they're looking for
- Four-year degree in medical, biological, physical, health, pharmacy, or related science
- Or two-year degree/nursing credential plus relevant life science experience
- Strong project management and organizational planning skills
- Understanding of ICH GCP guidelines and FDA/EU clinical trial regulations
- Proficiency in Microsoft Office applications
- Ability to manage multiple concurrent tasks in fast-paced environment
- Strong written and oral communication skills
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 on-time and on-budget project completion
- Manage compilation, tracking, and analysis of site activation deliverables
- Develop and maintain site activation project plans with assigned team members
- Report project status to sponsors and leadership; escalate risks and issues proactively
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.