Senior Clinical Research Associate - Oncology (US, West Coast)

Worldwide Clinical Trials seeks a Senior Clinical Research Associate to manage oncology clinical trials across West Coast investigative sites. The role involves site qualification, monitoring visits, protocol adherence oversight, and regulatory compliance throughout the trial lifecycle, with approximately 8-10 days of monthly travel.

Responsibilities

• Manage clinical research activities and site performance at investigative sites
• Conduct pre-site selection, initiation, interim, and closeout monitoring visits
• Coordinate study start-up activities including regulatory documentation and contracts
• Train site personnel on protocol requirements, data collection, and safety reporting
• Ensure compliance with informed consent, safety reporting, and regulatory standards

Requirements

• Bachelor's degree or nursing degree
• 5+ years as regional, traveling Clinical Research Associate
• Oncology clinical trial monitoring experience; hematology preferred
• Full-service monitoring experience preferred
• Strong knowledge of clinical trial processes and regulatory requirements
• Ability to travel 8-10 days monthly within West Coast region

Compensation: $97,000–$193,000 base annually