Senior Clinical Research Associate – Oncology
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Job Description
Senior CRA monitoring oncology clinical trials for Worldwide Clinical Trials, a global CRO. Managing investigative sites, regulatory compliance, data quality, and safety across the Northeast.
Responsibilities:
- Manage clinical research activities at investigative sites participating in Worldwide Clinical Trials studies
- Identify and assess potential research sites
- Coordinate study start-up activities, including regulatory documentation and contract and budget processes
- Conduct PSSVs, SIVs, IMVs, and COVs
- Train site personnel on protocols, data collection, and safety reporting
- Monitor site performance and provide ongoing study maintenance support
- Ensure informed consent, safety reporting, and regulatory compliance
- Partner with sites and study teams to drive data quality, participant safety, and study success
- Support site closeout activities and completion of study requirements
Requirements:
- Bachelor's Degree or a Nursing Degree
- 5+ years as a regional, traveling Clinical Research Associate
- Required experience monitoring Oncology clinical trials
- Requires travel within the specified region; 8–10 DOS monthly, with some visits remote
- Experience in full-service monitoring preferred
- Strong knowledge of clinical trial processes, site management, and regulatory requirements
- Candidates must reside within the Northeastern United States
- Ability to travel to investigative sites approximately 8–10 days per month
Benefits:
- Competitive benefits package depending on location
- Inclusive and equitable workplace
- Growth and learning opportunities
- Collaborative and inclusive environment
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