Scientific Director

Job Summary

Providing scientific and clinical input for early and late-stage oncology clinical development programs, the remote contract Scientific Director will manage protocol-specific and medical data review activities while collaborating with internal teams to design and execute study protocols.

Key responsibilities

• Partner with study teams to execute clinical studies and develop innovative clinical development plans
• Review and maintain clinical trial protocols, informed consent documents, and clinical study reports
• Provide scientific expertise for regulatory filings and author internal clinical documents for conferences

Required qualifications

• Advanced Clinical/Science Degree (e.g. MD, Pharm.D., Ph.D., MSN) required; Master's degree may be considered with relevant experience
• Minimum of 5 years of experience in clinical science, clinical research, or clinical development in oncology
• Proficient knowledge of oncology, clinical data analysis, GCP/ICH guidelines, and study design
• Strong organizational and project management skills with the ability to operate autonomously
• Effective communication skills for conveying clinical and scientific data to diverse audiences