Senior Clinical Research Associate (Oncology)

Responsibilities

• Independently monitor Phase II-III Oncology clinical trials in accordance with ICH-GCP guidelines, study protocols, and SOPs
• Conduct site initiation, routine monitoring, and close-out visits, averaging approximately 8 onsite monitoring days per month
• Perform source data review (SDR), source data verification (SDV), and case report form (CRF) review to ensure accurate, high-quality, inspection-ready data
• Partner closely with investigative sites to support patient enrollment, protocol adherence, and issue resolution
• Identify site-level risks and escalate concerns appropriately to maintain study quality and timelines
• Collaborate directly with biotech sponsors and cross-functional study teams to ensure successful clinical trial execution
• Manage multiple sites, study activities, and priorities while working independently with minimal oversight

Requirements

• Experience as a Senior Clinical Research Associate supporting Oncology clinical trials
• Strong background in independent site monitoring and clinical trial oversight
• Experience supporting Phase II and/or Phase III studies
• Comprehensive knowledge of ICH-GCP guidelines and clinical research regulations
• Ability to work directly with biotech sponsors in a client-facing environment
• Strong organizational, communication, and problem-solving skills
• Ability to manage multiple sites and competing priorities with minimal supervision
• Must reside within one hour of a major airport and be able to travel regionally
• Must be authorized to work in the United States

Pay

Competitive salary plus bonus, depending on experience

Schedule

Remote work environment with regional travel requirements