Senior CRA - Oncology

Responsibilities

• Oversee Phase II–III oncology studies independently, ensuring adherence to ICH-GCP guidelines, study protocols, and internal SOPs
• Perform on-site monitoring visits (approximately 8 days monthly), including site initiation, interim monitoring, and close-out activities
• Conduct source data verification/review and case report form assessments to maintain audit-ready data quality
• Build strong partnerships with investigative sites to drive enrollment, ensure protocol compliance, and resolve operational challenges
• Proactively identify site risks, escalate issues, and ensure milestones and study deliverables remain on track

Qualifications

• Proven experience as a Senior CRA with a focus on oncology clinical trials
• Demonstrated expertise in independent monitoring and full lifecycle trial oversight
• Prior experience working directly with biotech sponsors in a client-facing capacity
• Ability to manage multiple clinical sites and competing priorities with limited supervision
• Hands-on oncology site monitoring experience

Compensation

Salary range: Based on Experience
Comprehensive benefits package including medical, dental, vision, and retirement plans
Remote flexibility with regional travel requirements