Senior Clinical Research Associate - Oncology (US)
Worldwide Clinical Trials
Senior Clinical Research Associate for oncology studies at a global CRO. Manages research activities across participating clinical trial sites, from initiation through closeout, with a focus on regulatory compliance and safety reporting. Requires 5+ years CRA experience and oncology background.
Responsibilities
- Manage research activities and oversee compliance at assigned clinical trial sites
- Conduct study initiation visits and support site setup including regulatory documentation and contract negotiation
- Train sites on proper data collection and safety event reporting procedures
- Monitor site activities during study execution and manage closeout activities
- Ensure informed consent compliance and adherence to regulatory requirements
Requirements
- 5+ years of Clinical Research Associate experience
- 4-year university degree or nursing degree
- Oncology clinical trial experience required
- Proficiency in Microsoft Office, CTMS, and EDC systems
- Excellent written and oral English communication skills
- Superior organizational skills with strong attention to detail
- Willingness to travel regionally; U.S. residency required
Vacancy posted 1 day ago
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