Associate Director Clinical Science

• Support oncology clinical development programs, initially focused on prostate cancer with exposure to additional solid tumor studies
• Lead clinical data review, analysis, and medical monitoring activities to support study execution and patient safety
• Contribute to key clinical and regulatory deliverables, including protocols, CSRs, IBs, and regulatory submissions
• Partner closely with Clinical Operations, Regulatory, Biostatistics, Data Management, and other cross-functional teams
• Interpret clinical data, identify trends, and generate scientific insights to inform development decisions
• Ideal for a hands-on Clinical Scientist who enjoys wearing multiple hats in a lean, fast-paced biotech environment
• Strong preference for candidates with oncology experience, particularly in solid tumors, and a passion for advancing innovative cancer therapies

Desired Skills and Experience

• Seeking candidates with 5+ years of experience in Clinical Science, Clinical Development, or a closely related function within biotech or pharma.

• Strong background supporting oncology programs, particularly in solid tumors

• Experience contributing to study oversight through clinical data evaluation, safety review, and cross-functional collaboration.

Track record of supporting key clinical development deliverables and health authority submissions throughout the drug development lifecycle.

• Familiarity with developing study-level and regulatory documentation, including protocols, study reports, and other submission-related materials.

• Experience supporting BLA preparation or regulatory filings is a plus.

• Experience working within a small to mid-sized biotechnology company is preferred.