Medical Director - Clinical Oncology

Takeda Pharmaceutical

4-5 years

Not Disclosed

Mumbai

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

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Medical Director - Clinical Oncology

Job Description

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