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Clinical Medical Manager - Ahmedabad / Mumbai

4+ years
Not Disclosed
10 Dec. 2, 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: Clinical Medical Manager
Category: Medical Affairs
Locations: Ahmedabad / Mumbai, India
Department: Clinical Development Centre – India
Company: Novo Nordisk India Pvt. Ltd.


About Novo Nordisk

Novo Nordisk is a global healthcare company dedicated to defeating serious chronic diseases and improving patients’ lives. With over a century of innovation, the company fosters a patient-centered approach, leveraging scientific excellence, cross-functional collaboration, and data-driven strategies to bring innovative therapies to market.


Role Overview

As a Clinical Medical Manager, you will be part of a high-performing Clinical Medical team, driving clinical development strategy and execution for Novo Nordisk’s pipeline in India. You will build scientific relationships, deliver clinical insights, and implement strategies that influence clinical trial outcomes and early portfolio development.


Key Responsibilities

Clinical Trial Excellence:

  • Provide scientific and medical input for early trial planning, start-up, recruitment, and retention.

  • Collaborate with Clinical Operations Therapy Area Leads and Trial Managers on clinical trial strategies.

  • Monitor trial performance and proactively address scientific issues.

  • Engage with site staff to ensure compliance and smooth trial conduct.

Scientific Engagement & Stakeholder Management:

  • Act as local subject matter expert on products and trial protocols.

  • Build and maintain relationships with Principal Investigators (PIs) and other key stakeholders.

  • Contribute to site selection, scientific training, and assessment of medical capabilities.

  • Communicate pipeline and scientific narratives effectively to internal and external stakeholders.

Organizational Readiness & Capability Building:

  • Collaborate with Therapy Area Leads to co-design scientific knowledge building for Clinical Operations.

  • Introduce Medical Affairs colleagues to KOLs and new therapy areas.

  • Support early portfolio strategy, pre-launch planning, and capability development.

Travel:

  • Periodic travel to clinical trial sites within the assigned region and to the India Head Office as required.


Qualifications & Experience

  • M.B.B.S with M.D. in a relevant discipline, strong clinical practice or research background.

  • 4+ years’ experience in clinical or medical affairs strategic roles in the pharmaceutical industry.

  • Strong knowledge of pharmaceutical drug development, ICH-GCP guidelines, regulatory requirements, and clinical trial methodology.

  • Proven ability to build scientific relationships, influence stakeholders, and implement innovative strategies.

  • Excellent written, verbal, and presentation skills.

  • Willingness to adopt AI tools and data-driven approaches in work.

  • Ability to travel periodically for site visits and align with organizational priorities.


Skills & Competencies

  • Strategic thinker with enterprise mindset and cross-functional collaboration.

  • Strong stakeholder management and external engagement skills.

  • Adaptable, innovative, and able to embrace change.

  • Demonstrates accountability, urgency, and solution-oriented approach.

  • Ability to thrive in a dynamic, fast-paced environment.


About Clinical Development Centre – India (CDC-India)

The CDC-India is part of the Clinical, Medical, and Regulatory (CMR) department. Clinical Medical Managers play a vital role in driving clinical trial excellence, early portfolio strategies, and scientific leadership while maintaining a patient-centered focus. The CDC-India collaborates across functions to ensure successful execution of pipeline products and patient impact.


Working at Novo Nordisk

  • Unconventional, innovative, and patient-focused culture.

  • Opportunities for learning, career growth, and cross-functional collaboration.

  • Competitive compensation and benefits tailored to career and life stage.

  • Inclusive recruitment process and commitment to equality of opportunity.


Application & Deadline

  • Submit CV and motivational letter online via the Novo Nordisk career portal.

  • Deadline: 11th December 2025

Note: Novo Nordisk warns against fraudulent job offers. They do not charge fees or request funding as part of recruitment.