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Associate Director Clinical Science
Job in
Boston, Suffolk County, Massachusetts, 02298, USA
Listed on 2026-10-12
Listing for:
EPM Scientific
Full Time
position Listed on 2026-10-12
Job specializations:
-
Science
Clinical Research, Oncology Care
Job Description & How to Apply Below
- 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
- 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
- - 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.
Position Requirements
10+ Years
work experience
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