Senior Clinical Research Associate – Oncology
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Job Description
Senior CRA conducting oncology clinical trials for Worldwide Clinical Trials, a global CRO. Managing site monitoring, regulatory compliance, and study delivery across the Western United States.
Responsibilities:
- Manage clinical research activities at investigative sites participating in Worldwide clinical studies
- Identify and assess potential research sites
- Coordinate study start-up activities, including regulatory documentation and contract and budget processes
- Conduct Pre-Site Selection, Study Initiation, Interim Monitoring, and Closeout Visits
- Train site personnel on protocol requirements, 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
- Collaborate with sites, sponsors, and global study teams
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 Western United States territory
- Ability to travel to investigative sites approximately 8–10 days per month
Benefits:
- Competitive benefits package depending on location
- Inclusive and equitable workplace
- Equal employment opportunities
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