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Senior Medical Director, Clinical Science - Oncology

5-7 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

🧠 Job Title: Senior Medical Director, Clinical Science – Oncology

Job ID: R0163072
Date Posted: September 17, 2025
Location: Mumbai, Maharashtra, India
Company: Takeda Pharmaceuticals
Employment Type: Full-time | Regular | Hybrid
Job Level: Senior
Travel Requirement: 15–25% (Minimal to Moderate)


🌟 About Takeda

For over 240 years, Takeda has been translating science into breakthrough medicines. As a values-led, R&D-driven global biopharmaceutical leader, Takeda focuses on transformative therapies that make a lasting impact on millions of patients worldwide.

In our R&D division, innovation thrives in a diverse, collaborative, and inclusive environment that amplifies every voice and empowers individuals to contribute to Better Health and a Brighter Future.

Join a trusted global organization where your scientific expertise and leadership will accelerate innovation and drive meaningful change.

🔗 Learn more: Takeda Careers


🎯 Position Objective / Purpose

  • Lead and strengthen Oncology Therapeutic Area Unit (OTAU) R&D capabilities in India

  • Align India’s oncology operations with global OTAU R&D goals

  • Drive speed and quality in clinical execution across India

  • Partner with regional/global leaders to enhance clinical trial acceleration

  • Oversee Clinical Science activities and strategic R&D initiatives in India


🧩 Key Responsibilities

🔹 1. Leadership & Strategy

  • Lead India OTAU R&D strategy and execution in alignment with global objectives

  • Collaborate with Global Project Teams (GPTs) and R&D functions on India development plans

  • Monitor India’s oncology performance, feasibility, and site selection

  • Serve as internal expert on India’s oncology landscape

  • Foster collaboration between India LOC, OTAU-China, OTAU-Japan, and global teams

🔹 2. Clinical Development & Execution

  • Lead and mentor Clinical Science teams in India

  • Direct Development Team strategy, including Clinical Development Plans (CDPs) and protocols

  • Oversee clinical trial design, execution, and interpretation

  • Ensure regulatory alignment and data integrity

  • Accountable for timely delivery, budget oversight, and risk mitigation

🔹 3. Medical Oversight & Data Interpretation

  • Oversee medical monitoring and patient safety assessments

  • Review and interpret clinical and safety data

  • Partner with Pharmacovigilance on safety signal assessment

  • Support Health Authority interactions and regulatory submissions

🔹 4. External Engagement

  • Develop and maintain strong KOL networks and investigator relationships

  • Represent Takeda in scientific, clinical, and regulatory discussions

  • Support regulatory strategy and clinical submissions in India

🔹 5. Due Diligence & Business Development

  • Lead due diligence for potential alliances or in-licensing opportunities

  • Evaluate scientific and strategic fit of partnership assets

  • Act as clinical representative in global business development teams

🔹 6. People Leadership

  • Build and lead a high-performing oncology clinical science team

  • Mentor and develop team members; foster engagement and growth

  • Drive performance management, career development, and well-being initiatives

🔹 7. Local Advocacy & Escalation

  • Serve as country subject matter expert (SME) for oncology R&D

  • Address and resolve complex local issues or investigator concerns

  • Engage with India’s innovation ecosystem to explore collaborative opportunities


🎓 Education & Experience Requirements

🎓 Education

  • MD, MD/PhD, or internationally recognized equivalent

  • Clinical training in Malignant Hematology and/or Medical Oncology preferred

💼 Experience

  • 5–7 years of clinical research experience in pharma, CRO, consulting, or academia

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

  • Proven success in leading multi-regional/global development teams

  • Experience with NDA/MAA submissions preferred


💡 Skills & Competencies

  • Deep understanding of Oncology therapeutic areas and mechanisms of action

  • Strong grasp of ICH GCP, regulatory compliance, and local regulations

  • Proven strategic, communication, and negotiation skills

  • Proactive risk management and problem-solving abilities

  • Expertise in clinical development, medical monitoring, and regulatory strategy

  • Ability to navigate matrixed organizations and drive cross-functional decisions

  • Fluency in English (oral and written) with strong medical writing capabilities

  • Awareness of emerging research trends and global development standards


🌍 Travel Requirements

  • Travel: 15–25% (Domestic & International)

  • Includes meetings, site visits, and investigator engagement


🌈 Diversity, Equity & Inclusion

Takeda is proud to be an Equal Opportunity Employer, committed to a diverse workforce and inclusive culture.
Employment decisions are made without regard to race, color, religion, gender, sexual orientation, gender identity, national origin, disability, age, or veteran status.

This position is classified as Hybrid under Takeda’s Hybrid and Remote Work Policy.


🧭 Work Type

  • Worker Type: Employee

  • Sub-Type: Regular

  • Time Type: Full-time

  • Location: Mumbai, India