Medical Director - Oncology

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 Responsibilities1. Clinical Trial LeadershipDesign and execute Phase 1–3 oncology trialsDevelop study protocols aligned with the overall clinical development strategyEnsure trials are scientifically sound, efficient, and patient-focused2. Medical Oversight & Safety MonitoringAct as the medical lead for ongoing trialsReview:Patient eligibilitySafety dataAdverse eventsWork closely with pharmacovigilance teams to ensure patient safety3. Data Analysis & InterpretationInterpret clinical trial results:SafetyEfficacyPharmacokinetics (PK/PD)Patient-reported outcomesTranslate findings into meaningful conclusions for regulatory and clinical use4. Regulatory & Documentation WorkContribute to:Clinical study reportsRegulatory submissionsRespond to queries from:Health authoritiesEthics committees5. Cross-Functional CollaborationWork in a matrix team with:ScientistsRegulatory affairsBiostatisticiansToxicology & pharmacology teams6. External Engagement & Thought LeadershipBuild relationships with Key Opinion Leaders (KOLs) and researchersCollaborate with investigators on:Publications (papers, posters, abstracts)Represent the company in scientific discussions and partnerships7. Strategic ContributionContribute to:Disease-area strategiesClinical development plansLifecycle management of drugsUnderstand:Cancer biologyCompetitive landscapeTreatment guidelinesKnowledge/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 desirableExperience RequirementsMinimum:3+ years in pharma/biotech OR relevant clinical researchExperience in clinical trials (design, execution, or participation)Publication or clinical practice historyPreferred:5+ years industry experienceExperience leading oncology trialsStrong understanding of:Drug development processRegulatory requirements (GCP)Oncology landscape