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Team Lead- Medical Affairs

6-8 years
Not Disclosed
10 Nov. 13, 2025
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ 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: Team Lead – Medical Affairs (Oncology)

Location: Hyderabad
Department: Medical Affairs & Information
Business Unit: Global Generics India (GG India)


Company Overview

Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company with a presence in over 66 countries and more than 24,000 employees. Founded in 1984, we are driven by a single purpose: to accelerate access to affordable and innovative medicines — because Good Health Can’t Wait.

For nearly four decades, we have stood for access, affordability, and innovation, underpinned by deep science, progressive people practices, and robust governance. As the industry evolves, we continue to strengthen our core businesses while building for the future — guided by our strategy “The Next and the New.”

Our goal is to reach 1.5+ billion patients globally by 2030, through sustainable growth that respects people, planet, and purpose.
We are an equal opportunity employer, committed to diversity, inclusion, and a discrimination-free workplace.


Job Summary

The Team Lead – Medical Affairs (Oncology) will serve as the scientific, technical, and ethical anchor for all medical activities related to the oncology portfolio.
This role involves strategic leadership, people management, and cross-functional collaboration to support product commercialization, scientific engagement, clinical research, sales training, and compliance.

The position requires deep expertise in Oncology and Medical Affairs, along with the ability to manage teams, shape strategy, and drive business objectives with scientific integrity.


Key Responsibilities

1. Strategic & Tactical Leadership

  • Provide strategic and operational inputs to Product Management and Marketing teams for ethical and evidence-based promotion.

  • Contribute to brand plans, review and approve promotional and educational materials, ensuring compliance with internal SOPs and regulatory codes.

  • Support cluster head in budgeting, resource allocation, and expense control.

2. Medical & Scientific Support

  • Develop and approve clinical protocols, trial designs, and study documents in collaboration with Global Medical Affairs and Clinical Development.

  • Provide medical expertise for safety reporting, NDA planning, and local study support.

  • Ensure accurate and balanced medical information delivery to internal and external stakeholders.

3. Product Commercialization & Launch Support

  • Partner with the New Product Planning team for business case preparation and pre-commercialization activities.

  • Support market research, stakeholder mapping, and early access programs.

  • Provide medical inputs for regulatory submissions, labelling documents, and adverse event processing.

  • Contribute to new product launches, particularly in Oncology.

4. Training & Capability Building

  • Lead scientific and product training for the sales force and new product launches.

  • Foster a learning and development culture within the Medical Affairs team.

  • Provide guidance and mentorship to team members to ensure alignment with company values.

5. Stakeholder & KOL Engagement

  • Serve as the primary Medical Affairs contact for Customer Relationship Management.

  • Facilitate collaborations and communications with healthcare professionals, academic institutions, and external experts.

  • Build and maintain relationships with key opinion leaders (KOLs) to support medical initiatives.

6. Cross-functional Collaboration

  • Partner with teams across Regulatory Affairs, Clinical Development, Pharmacovigilance, and Quality for product lifecycle management.

  • Support business development activities including evaluations for licensing, acquisitions, and co-promotions.


Qualifications & Experience

Education:

  • Postgraduate degree in Pharmacology or a related medical specialty OR

  • Graduate degree in Medicine (MBBS/MD or equivalent)

Experience:

  • 6–8 years of relevant experience in Medical Affairs or as a Medical Advisor

  • Minimum 3 years of experience in Oncology Therapeutic Area

  • Prior experience in new product launches in Oncology


Skills & Attributes

Technical Skills

  • In-depth understanding of pharmaceutical R&D, commercialization, and medical governance.

  • Strong knowledge of clinical pharmacology, trial design, medical statistics, and therapeutic area expertise.

  • Familiarity with industry codes, SOPs, and regulatory compliance frameworks.

Behavioral & Leadership Skills

  • Excellent communication and presentation skills.

  • Strong analytical and decision-making abilities.

  • Effective interpersonal skills for cross-functional and external collaboration.

  • Proven ability to influence, lead, and develop teams.


About Global Generics India

The Global Generics India business, established in 1986, ranks among the top 10 pharmaceutical companies in India (as per IQVIA MAT, Nov 2022).
We are a fast-growing organization with a strong presence across therapy areas including Oncology, Anti-allergy, and Gastrointestinal diseases.
Our mission is to leverage digital transformation, collaborations, and innovation to become one of the top 5 players in the Indian Pharma Market.


Employee Benefits

  • Competitive compensation and benefits package aligned with industry standards

  • Relocation and joining support

  • Family-friendly policies (maternity, paternity, and parental benefits)

  • Medical and life coverage for employee and family

  • Continuous learning and development programs