Instagram
youtube
Facebook

Medical Director - Clinical Oncology

4-5 years
Not Disclosed
10 Sept. 30, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

🌐 Position: Medical Director – Clinical Oncology

Location: Mumbai, Maharashtra
Job Type: Full-Time | Senior Level
Travel: Minimal (15–25%)
Company: Takeda Pharmaceuticals
Job ID: R0158310
Date Posted: July 16, 2025


🧭 Objective / Purpose

  • Strengthen and lead Oncology Therapeutic Area Unit (OTAU) R&D capabilities in India.

  • Maximize value by accelerating global innovation and efficiency aligned with global OTAU R&D goals.

  • Oversee and ensure effective oncology operations in India, leveraging local opportunities.

  • Collaborate with global OTAU teams (India, China, Japan) and R&D functions for speed and quality.

  • Partner with ISEA and India LOC leaders to enhance enterprise-level global clinical trial acceleration.


🎯 Key Accountabilities

1. India R&D Strategy and Execution

  • Develop and execute integrated India development strategies in alignment with global teams.

  • Monitor country performance; support feasibility, site selection, and milestone achievement.

  • Serve as internal expert on India’s clinical development landscape.

  • Collaborate with India LOC to execute One Oncology Strategy, leveraging local expertise.

  • Build and maintain investigator networks for current and future oncology trials.

  • Scale global clinical trial capabilities in India for enhanced innovation and efficiency.


2. Clinical Development Leadership

  • Lead India Development Teams for assigned oncology compounds.

  • Oversee Development Strategy, Clinical Development Plans, and Clinical Protocols.

  • Identify risks, contingencies, and mitigation strategies proactively.

  • Guide India-specific strategic decisions and “Go / No-Go” recommendations.

  • Ensure development strategies are competitive and regulatory-compliant.


3. Protocol Development, Study Execution & Data Interpretation

  • Lead Oncology Clinical Science activities in India.

  • Accountable for protocol development, study execution, and data interpretation.

  • Advise clinical scientists and ensure timely project completion.

  • Interpret data scientifically and clinically for medical significance.


4. Trial Medical Monitoring

  • Oversee medical monitoring activities during trials.

  • Assess safety-related issues and protocol conduct.

  • Collaborate with Pharmacovigilance on safety assessments.


5. External Stakeholder Engagement

  • Lead KOL and investigator engagement strategies.

  • Contribute to regulatory strategy and liaise with authorities in India.

  • Act as advisor and representative to senior leadership on external collaborations.


6. Due Diligence & Business Development

  • Participate in due diligence evaluations for business development or in-licensing opportunities.

  • Assess scientific, medical, and strategic feasibility of potential assets.

  • Represent clinical science in BD alliances and negotiations.

  • Serve as clinical point of contact for alliance projects and partnerships.


7. Leadership & Team Development

  • Build, manage, and mentor the India OTAU Clinical Science team.

  • Foster a high-performance culture focused on innovation, collaboration, and well-being.

  • Represent OTAU on cross-functional task forces and strategic committees.

  • Drive performance management, career development, and engagement initiatives.


8. India Country Expertise & Advocacy

  • Act as country matter expert for oncology R&D in India.

  • Serve as a bridge between global R&D and India’s innovation ecosystem.

  • Lead escalations for country-specific operational or investigator-related issues.

  • Develop India oncology strategies based on business and research needs.


🎓 Education & Competency Requirements

🎓 Education

  • MD, or MD/PhD (or internationally recognized equivalent).

  • Specialization preferred: Malignant Hematology and/or Medical Oncology.

💼 Experience

  • 3–5 years in clinical research (pharma, CRO, consulting, or academia).

  • 4–5 years of people management experience in life sciences.

  • Proven record in leading global/regional clinical development teams.

  • Experience in multi-regional studies, including beyond US/EU.

  • Experience with NDA/MAA submissions preferred.

  • Knowledge of India’s clinical trial management and regulatory support processes.

🧠 Knowledge

  • Deep understanding of oncology therapeutic areas and mechanisms of action.

  • Strong knowledge of global and local regulatory requirements (ICH-GCP).

  • Awareness of emerging research trends in oncology.

💡 Skills

  • Strategic leadership and decision-making in matrixed environments.

  • Excellent communication, negotiation, and interpersonal abilities.

  • Strong medical writing and documentation skills.

  • Cultural sensitivity and positive influencing across diverse regions.

  • Proficiency in business English (written and spoken).


✈️ Travel Requirements

  • Occasional domestic and international travel (approx. 15–25%).

  • Travel for meetings, site visits, and collaborations.


📍 Work Details

  • Location: Mumbai, India

  • Worker Type: Employee (Regular)

  • Time Type: Full-time