Senior CRA Oncology Contract

Responsibilities

• Perform site monitoring visits across study phases, ensuring compliance with protocol, regulatory requirements, and GCP standards
• Maintain direct communication with investigative sites, providing guidance and resolving study-related challenges
• Oversee oncology study activities by reviewing data quality, patient safety measures, and overall site performance
• Manage multiple trial sites simultaneously, prioritizing deliverables and tracking key study milestones
• Collaborate with biotech sponsors and internal teams to support efficient and timely trial execution

Requirements

• 5+ years of CRA experience with at least 2+ years supporting oncology clinical trials
• Strong experience with independent monitoring and full clinical trial lifecycle management
• In-depth knowledge of ICH-GCP guidelines, FDA regulations, and oncology protocols
• Experience working directly with biotech or sponsor clients in a fast-paced environment
• Able to manage multiple priorities effectively with approximately 25–40% travel

Compensation

$60 – $80/hour
Contract role
Travel reimbursement provided