The Medical Director – Oncology Clinical Development is a senior physician-scientist role responsible for designing, leading, and overseeing clinical trials (Phase 1–3) for new cancer treatments. The goal is to bring innovative oncology drugs from early development to regulatory approval and market launch.

Core Responsibilities 1. Clinical Trial Leadership Design and execute Phase 1–3 oncology trials Develop study protocols aligned with the overall clinical development strategy Ensure trials are scientifically sound, efficient, and patient-focused 2. Medical Oversight & Safety Monitoring Act as the medical lead for ongoing trials Review: Patient eligibility Safety data Adverse events Work closely with pharmacovigilance teams to ensure patient safety 3. Data Analysis & Interpretation Interpret clinical trial results: Safety Efficacy Pharmacokinetics (PK/PD) Patient-reported outcomes Translate findings into meaningful conclusions for regulatory and clinical use 4. Regulatory & Documentation Work Contribute to: Clinical study reports Regulatory submissions Respond to queries from: Health authorities Ethics committees 5. Cross-Functional Collaboration Work in a matrix team with: Scientists Regulatory affairs Biostatisticians Toxicology & pharmacology teams 6. External Engagement & Thought Leadership Build relationships with Key Opinion Leaders (KOLs) and researchers Collaborate with investigators on: Publications (papers, posters, abstracts) Represent the company in scientific discussions and partnerships 7. Strategic Contribution Contribute to: Disease-area strategies Clinical development plans Lifecycle management of drugs Understand: Cancer biology Competitive landscape Treatment guidelines

Knowledge/Education Required: MD (or equivalent)-board certification or board qualifications in medical oncology, radiation oncology, hematology or internal medicine (with hematology or oncology experience) MD (or equivalent) plus other relevant advanced or Masters level degree (e.g., PhD, MBA, MPH etc)-Licensure to practice medicine in the respective jurisdiction of the candidate is desirable

Experience Requirements Minimum: 3+ years in pharma/biotech OR relevant clinical research Experience in clinical trials (design, execution, or participation) Publication or clinical practice history Preferred: 5+ years industry experience Experience leading oncology trials Strong understanding of: Drug development process Regulatory requirements (GCP) Oncology landscape