Senior Clinical Research Associate - Rare Disease or Oncology - East Coast/Central
Worldwide Clinical Trials · Virtual United States Texas +1 more
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Senior Clinical Research Associate position overseeing site management and regulatory compliance for rare disease and oncology clinical trials. Remote role based on East Coast or Central US, requiring extensive experience managing research activities across trial phases and regional travel.
What they're looking for
- 5+ years experience as a Clinical Research Associate
- 4-year university degree or nursing degree
- Rare disease or oncology therapeutic area experience required
- Proficiency in Microsoft Office, CTMS, and EDC systems
- Excellent written and oral communication skills in English
- Superior organizational skills with attention to detail
- East Coast or Central US residency with willingness to travel regionally
What you'll be doing
- Manage research activities and compliance at clinical trial sites
- Conduct study initiation visits and oversee site start-up activities including regulatory documentation
- Train sites on proper data collection and safety event reporting procedures
- Monitor site performance during study maintenance and manage study closure activities
- Ensure informed consent compliance and adherence to regulatory requirements
Compensation$97,000.00 - $193,000.00 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.