Senior Clinical Research Associate - Oncology - Midwest
Worldwide Clinical Trials · Virtual United States Wisconsin +1 more
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Senior Clinical Research Associate position managing oncology clinical trial sites across the Midwest. Responsible for site selection, study initiation, regulatory compliance, data management, and site closeout activities, with both remote and regional travel components.
What they're looking for
- 5+ years clinical research associate experience
- 4-year university degree or nursing degree
- Current oncology experience; CAR-T experience preferred
- Proficiency in Microsoft Office, CTMS, and EDC systems
- Fluent written and verbal English
- Superior organizational skills and attention to detail
- Ability to work independently with minimal supervision
What you'll be doing
- Manage research activities and compliance at assigned clinical trial sites
- Conduct study initiation visits and support site training on data collection procedures
- Coordinate regulatory documentation, contract negotiation, and budget management with sites
- Monitor site activities for safety reporting and regulatory adherence throughout study duration
- Ensure informed consent and protocol compliance across assigned sites
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.