Clinical Scientist III

Job Summary

Providing scientific and clinical input to oncology clinical development programs, the remote Clinical Scientist III will manage protocol-specific data review activities, collaborate with study teams, and assist in regulatory communications on a contract basis.

Key responsibilities

• Collaborate on the design, implementation, and execution of study protocols while reviewing data from assigned clinical trials
• Develop and maintain clinical trial protocols, manuals, and study reports, ensuring compliance with regulatory requirements
• Provide scientific expertise for regulatory filings and author internal clinical documents for scientific conferences

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, clinical research, or clinical development, specifically in oncology
• Proficient knowledge of oncology, clinical data analysis, GCP/ICH guidelines, and regulatory requirements for clinical studies
• Strong organizational and project management skills with the ability to operate autonomously
• Effective communication skills for conveying clinical and scientific data to diverse audiences