Senior Clinical Research Associate - Oncology (US, East Coast)
About The Position
Worldwide Clinical Trials is seeking a Senior Clinical Research Associate to support oncology clinical studies at investigative sites across the East Coast. This home-based role requires residence within the territory and approximately 8–10 days of travel per month, primarily regionally, with occasional travel to other locations as needed. The Senior CRA supports studies from site qualification through closeout, ensuring quality, patient safety, regulatory compliance, protocol adherence, timely data collection, and effective site performance. The role partners with investigative sites, sponsors, study teams, and global colleagues, providing monitoring, site-management support, guidance, and oversight throughout the clinical 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.
- Residence within the East Coast territory.
Nice To Haves
- Experience in full-service monitoring.
Responsibilities
- Manage clinical research activities at investigative sites participating in company studies.
- Identify and assess potential research sites to support successful study execution.
- Coordinate study start-up activities, including collection of regulatory documentation and support of 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 throughout study maintenance activities.
- Ensure compliance with informed consent requirements, safety reporting obligations, and applicable regulatory standards.
- Partner with sites and study teams to support data quality, participant safety, and study success.
- Support site closeout and ensure study requirements are completed at the conclusion of the trial.
Benefits
- Competitive benefits package, depending on location.
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What This Job Offers
Job Type
Full-time
Career Level
Senior
