Senior Director, Clinical Sciences
On-siteBoston, Massachusetts, United States
Job Summary
Lead and mentor a team of 4–6 Clinical Scientists while directly overseeing the design, execution, analysis, and interpretation of early- and late-stage oncology clinical trials. Ensure scientific rigor throughout study conduct by leading the development and review of key documents, including protocols, investigator brochures, and clinical study reports. Partner cross-functionally with Clinical Operations, Biostatistics, Regulatory Affairs, and Medical Writing to advance clinical development programs and interpret emerging clinical, safety, and biomarker data. Contribute scientific expertise to regulatory submissions and health authority interactions while establishing best practices to improve Clinical Science processes. Report to the Vice President, Clinical Development.
Required Qualifications
- MD, PhD, PharmD, MS within a relevant scientific discipline
- At least 12 years of experience in clinical science, or research
- At least 7 years of experience in oncology
- Demonstrated experience in designing and managing clinical trials
- Knowledge of regulatory guidelines and GCP
- Strong analytical skills
- Proficiency in statistical analysis
- Ability to interpret clinical data
- Excellent written and oral communication skills
- Experience working in a fast-paced environment
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