Oncology Clinical Scientist

Job Summary

Supporting oncology clinical development programs, the full-time remote Clinical Scientist, Associate Director will analyze clinical data, oversee medical monitoring, and contribute to regulatory documentation while collaborating with cross-functional teams.

Key Responsibilities

• Perform ongoing clinical data review and analysis to ensure data integrity and support safety and efficacy assessments
• Support medical monitoring activities, including review of adverse events and protocol deviations
• Author and contribute to key clinical and regulatory documents, including Clinical Study Reports and Investigator Brochures

Required Qualifications

• 5+ years of Clinical Scientist or related clinical development experience within biotechnology or pharmaceutical organizations
• Oncology clinical development experience required, with a focus on solid tumor studies preferred
• Hands-on experience with clinical data review and medical monitoring
• Experience authoring clinical and regulatory documents, including CSRs and protocols
• Experience within a small or mid-sized biotechnology company is preferred