Senior Clinical Research Associate - Oncology (US, West Coast)
About The Position
Worldwide Clinical Trials is hiring a home-based Senior Clinical Research Associate to support oncology clinical studies at investigative sites across the U.S. West Coast. The role requires residence within the territory and regional travel to sites approximately 8–10 days per month, with occasional travel to other locations as needed. The Senior CRA oversees clinical study activities from site qualification through closeout, ensuring quality, patient safety, regulatory compliance, protocol adherence, and reliable data collection. The role partners with investigative sites, sponsors, study teams, and global colleagues, providing site leadership, guidance, monitoring, and ongoing support throughout the trial lifecycle.
Requirements
- Bachelor's degree or nursing degree.
- At least 5 years of experience as a regional, traveling Clinical Research Associate.
- Experience monitoring oncology clinical trials.
- Ability to travel within the specified region, approximately 8–10 days per month.
- Strong knowledge of clinical trial processes, site management, and regulatory requirements.
- Reside within the U.S. West Coast territory.
Nice To Haves
- Hematology clinical trial monitoring experience.
- Experience in full-service monitoring.
Responsibilities
- Manage clinical research activities at investigative sites participating in Worldwide clinical studies.
- Identify and assess potential research sites to support successful study execution.
- Coordinate study start-up, including collecting regulatory documents and supporting contract and budget processes.
- Conduct Pre-Site Selection Visits (PSSVs), Study Initiation Visits (SIVs), Interim Monitoring Visits (IMVs), and Closeout Visits (COVs).
- Train site personnel on protocol requirements, data collection processes, and safety reporting expectations.
- Monitor site performance and provide ongoing support during study maintenance.
- Ensure compliance with informed consent requirements, safety reporting obligations, and applicable regulatory standards.
- Partner with sites and study teams to promote data quality, participant safety, and study success.
- Support site closeout and ensure study requirements are completed at trial conclusion.
Benefits
- Competitive benefits package, depending on location.
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What This Job Offers
Job Type
Full-time
Career Level
Senior
