Senior Director, Clinical Sciences

Responsibilities:
- Lead, mentor, and develop a team of 4–6 Clinical Scientists; provide balanced resource allocation across the clinical development portfolio.
- Hands-on leadership combining people leadership with direct scientific leadership of one or more clinical programs.
- Provide scientific leadership across the design, execution, analysis, and interpretation of early- and late-stage oncology clinical trials.
- Partner with Clinical Development physicians, Clinical Operations, Biostatistics, Clinical Pharmacology, Pharmacovigilance, Regulatory Affairs, Translational Medicine, and Medical Writing to ensure high-quality execution.
- Lead development and review of key clinical documents (protocols, investigator brochures, informed consent forms, clinical study reports, clinical development plans, regulatory briefing materials).
- Interpret emerging clinical, safety, PK/PD, and biomarker data to inform study conduct, dose selection, expansion opportunities, and development strategy.
- Contribute scientific expertise to regulatory submissions and health authority interactions.
- Ensure excellence in Clinical Science deliverables via best practices and continuous process improvement.
- Represent Clinical Science on cross-functional study teams, governance committees, and portfolio discussions.
- Foster a collaborative, accountable, scientifically rigorous culture.

Qualifications / What You Bring:
- MD, PhD, PharmD, or MS in a relevant scientific discipline.
- 12+ years of experience in clinical science or research.
- 7+ years of experience in oncology.
- Demonstrated experience designing and managing clinical trials; knowledge of regulatory guidelines and GCP.
- Strong analytical skills (statistical analysis and clinical data interpretation).
- Excellent written and oral communication skills.
- Experience working in a fast-paced environment.