Senior Clinical Research Associate - Oncology - East Coast
Worldwide Clinical Trials · Virtual United States Pennsylvania +1 more
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Worldwide Clinical Trials seeks a Senior Clinical Research Associate to manage oncology research activities at participating sites across the East Coast. The role involves study oversight from initiation through closure, including site management, regulatory compliance, and safety reporting.
What they're looking for
- 5+ years experience as a Clinical Research Associate
- 4-year university degree or nursing degree
- Oncology experience required
- Proficiency in Microsoft Office, CTMS, and EDC systems
- Excellent English communication and organizational skills
- East Coast residency with willingness to travel regionally
What you'll be doing
- Manage research activities at clinical trial sites, including site selection and contract negotiations
- Conduct study initiation visits and ensure regulatory document collection
- Train sites on data collection and safety event reporting procedures
- Monitor site compliance with informed consent and regulatory requirements during study maintenance
- Close out research activities upon study conclusion
Compensation$97,000–$193,000 annually
Key requirements
- Therapeutic area
- Oncology
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.