Remote Clinical Research Associate (Oncology)

Responsibilities

• Independently oversee Phase II–III oncology clinical trials, ensuring adherence to ICH-GCP guidelines, study protocols, and organizational SOPs.
• Execute on-site monitoring activities (approximately 8 days per month), including site initiation, interim monitoring, and close-out visits.
• Conduct comprehensive Source Data Review (SDR), Source Data Verification (SDV), and Case Report Form (CRF) reviews to maintain data accuracy, integrity, and inspection readiness.
• Collaborate closely with investigative sites to support patient enrollment efforts, ensure effective study execution, and proactively resolve operational challenges.
• Assess and mitigate site-level risks, escalating issues as needed to maintain study quality, compliance, and timeline objectives.
• Serve as a key liaison with biotech sponsors, demonstrating strong communication skills, adaptability, and a proactive, ownership-driven approach to study management.

Qualifications

• 3-5+ years of experience as a clinical researcher conducting on-site monitoring
• Experience as a Senior CRA supporting Oncology trials
• Strong background in independent monitoring and trial oversight
• Comfortable working directly with biotech clients
• Able to manage multiple sites and priorities with minimal oversight

Pay

Total compensation based on experience level - $120,000-$165,000+

Benefits

• PTO
• 11 Paid Holidays
• Medical, Dental, and Vision coverage
• 401k with ADP

Long-term Program

3.5 years remaining