Site Activation Manager
Worldwide Clinical Trials · Durham, NC
Clinical OperationsFull-timeCompany career page
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Role summary
Worldwide Clinical Trials seeks a Site Activation Manager to lead project management and delivery for oncology clinical studies. The role encompasses site identification, regulatory coordination, contract oversight, and cross-functional collaboration to ensure timely study initiation in compliance with GCP and applicable regulations.
What they're looking for
- Bachelor's degree or nursing degree required
- Minimum 4 years CRO experience in study start-up with country lead or manager experience
- Strong leadership and organizational management skills in planning and scheduling
- Understanding of regulatory processes, ICH GCP guidelines, and FDA/EU clinical trial directives
- Proficiency in MS Office applications and digital systems
- Cross-cultural communication and fluent English language skills
What you'll be doing
- Serve as primary accountability lead for site activation and start-up on assigned oncology studies
- Oversee cross-functional site activation activities to achieve milestones on time and within budget
- Manage tracking, analysis, and reporting of site activation progress and key metrics
- Communicate activation status, risks, and mitigation plans to sponsors and project leadership
- Ensure compliance with SOPs, ICH GCP, and applicable regulatory requirements
Compensation$86,000-$170,000
Privacy & handoff
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