Scientific Director

Job Summary

To support oncology clinical development programs, the contract Scientific Director will develop and maintain clinical trial protocols, review data from clinical trials, and collaborate with internal experts, all while working remotely.

Key responsibilities:

• Develop and maintain clinical trial protocols, manuals, and study reports
• Review clinical trial data and assist with data interpretation for internal and external stakeholders
• Collaborate with the Medical Director and study teams to design and execute clinical studies

Required qualifications:

• Advanced Clinical/Science Degree (e.g., MD, Pharm.D., Ph.D., MSN) required; a Master's degree may be considered with relevant industry experience
• Minimum of 5 years of experience in clinical science, research, or development, particularly in oncology
• Proficient knowledge of oncology, clinical data analysis, GCP/ICH, and regulatory requirements
• Ability to communicate clinical and scientific data effectively to diverse audiences
• Strong organizational and project management skills, with a high degree of autonomy