Site Activation Manager
Worldwide Clinical Trials · Remote
RoleLantern re-checked this role's application link recently and it was active — the employer has not confirmed it directly.
Role summary
Worldwide Clinical Trials seeks a Site Activation Manager to oversee study initiation and site activation activities within assigned therapeutic areas. The role manages coordination of site identification, contract monitoring, essential document collection, and regulatory compliance across clinical trial projects, reporting to senior leadership.
What they're looking for
- Four-year degree in medical, biological, physical, health, pharmacy, or related science
- Two-year nursing or life science degree with relevant clinical trial experience
- Understanding of ICH GCP guidelines and FDA/EU clinical trial regulations
- Project management experience in clinical trial initiation and planning
- Strong organizational and leadership skills with independent decision-making ability
- Proficiency in Microsoft Office applications and digital systems
- Ability to manage multiple tasks in fast-paced, deadline-driven environment
What you'll be doing
- Serve as primary contact for study start-up and maintenance activities on assigned projects
- Oversee site identification, qualification, and selection process and functional team activities
- Manage tracking, compilation, and analysis of site activation progress and metrics
- Develop risk assessments and mitigation plans; escalate issues to leadership as needed
- Communicate project status and budget matters to sponsors, teams, and stakeholders
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.