Associate Director Clinical Science

Support oncology clinical development programs, initially focused on prostate cancer with exposure to additional solid tumor studiesLead clinical data review, analysis, and medical monitoring activities to support study execution and patient safetyContribute to key clinical and regulatory deliverables, including protocols, CSRs, IBs, and regulatory submissionsPartner closely with Clinical Operations, Regulatory, Biostatistics, Data Management, and other cross-functional teamsInterpret clinical data, identify trends, and generate scientific insights to inform development decisionsIdeal for a hands-on Clinical Scientist who enjoys wearing multiple hats in a lean, fast-paced biotech environmentStrong 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.