Senior Medical Director

Job Summary

Providing medical oversight for clinical studies, the full-time Senior Medical Director will manage the design, implementation, and monitoring of Phase I-III Oncology clinical trials in a remote setting.

Key responsibilities:

• Design, author, and review clinical study documents including protocols and reports
• Act as a medical monitor and provide clinical input for protocol monitoring guidelines
• Track and inform the Clinical Development team of changes in drug efficacy and safety profiles during ongoing trials

Required qualifications:

• Medical Doctor (MD) with experience in solid tumor clinical trials; recent experience in breast carcinoma preferred
• 8-10 years of clinical development experience in the pharmaceutical or biotechnology industry
• Experience with Phase I-III clinical trials, with a preference for Phase 3 experience
• Thorough understanding of clinical trial design, methodology, and statistical concepts
• In-depth knowledge of GCP/ICH guidelines and the IND/NDA process