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Manager, Clinical Medical - Hyderabad

Novo Nordisk
Novo Nordisk
3-4 years
upto 9 LPA
Bangalore, India
10 April 24, 2026
Job Description
Job Type: Full Time Education: B.Pharm, M.Pharm, Pharm D., BSc., MSc. 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

Manager, Clinical Medical – Clinical Development Strategy


Location: Hyderabad, Telangana, India
Department: Clinical Development Centre – India (CDC-India)
Company: Novo Nordisk
Job Category: Medical Affairs
Employment Type: Full-Time
Application Deadline: 30 April 2026
Experience Required: Minimum 4+ years (Not suitable for freshers)


About the Company
Novo Nordisk is a globally leading healthcare organization with over a century of expertise in combating chronic diseases. Known for its innovation-driven approach and patient-centric philosophy, the company continues to redefine treatment standards and improve global health outcomes through cutting-edge clinical development and scientific excellence.


Job Overview
The Manager, Clinical Medical role is a strategic and high-impact position within the Clinical Development ecosystem. This role is designed for experienced medical professionals who can drive clinical trial excellence, contribute to early-stage pipeline strategy, and build strong scientific engagement with investigators and key stakeholders. You will play a pivotal role in shaping clinical strategies and ensuring successful trial execution across India.


Key Responsibilities

  • Drive clinical trial excellence through scientific leadership, insights, and external engagement

  • Collaborate with Clinical Operations Therapy Area Leads and Trial Managers across all trial phases including planning, start-up, recruitment, and retention

  • Provide scientific and medical input into trial portfolio strategy, feasibility assessments, and country allocation decisions

  • Conduct periodic site visits to evaluate clinical trial conduct, gather insights, and strengthen investigator relationships

  • Define and assess site selection criteria, including scientific capabilities and training requirements

  • Engage and build long-term relationships with Key Opinion Leaders (KOLs) and Principal Investigators

  • Act as the subject matter expert for product and protocol, supporting feasibility discussions and resolving medical queries during trials

  • Monitor trial performance and proactively address scientific and operational challenges

  • Support expansion into new therapy areas by establishing strong scientific presence and stakeholder engagement

  • Communicate scientific narratives and pipeline insights effectively to external stakeholders

  • Contribute to mapping clinical care pathways to enhance patient recruitment and retention strategies

  • Collaborate cross-functionally to build organizational readiness and scientific capability within teams

  • Facilitate knowledge exchange and introduce Medical Affairs teams to emerging KOL networks


Travel Requirements
This role requires periodic travel to clinical trial sites across India and occasional visits to the India Head Office based on business needs.


Required Qualifications and Skills

  • MBBS with MD in a relevant medical discipline

  • Minimum 4+ years of experience in Clinical Development, Medical Affairs, or strategic roles within the pharmaceutical industry

  • Strong understanding of drug development lifecycle and clinical trial methodology

  • In-depth knowledge of ICH-GCP guidelines and global regulatory requirements

  • Proven ability to manage stakeholders and influence cross-functional teams

  • Excellent communication, presentation, and scientific storytelling skills

  • Strong analytical mindset with ability to interpret clinical data and derive actionable insights

  • Ability to adapt to evolving environments and drive continuous improvement initiatives

  • Experience or willingness to leverage AI-driven tools and data-based decision-making approaches


About the Department
The Clinical Development Centre-India (CDC-India) is a core part of the Clinical, Medical, and Regulatory (CMR) division at Novo Nordisk. This team operates at the intersection of science, strategy, and execution—playing a critical role in advancing clinical programs, strengthening investigator networks, and delivering scientific leadership across therapeutic areas. The department thrives on collaboration, innovation, and a strong patient-first approach.


Why Join Novo Nordisk

  • Be part of a globally respected healthcare organization with over 100 years of impact

  • Work on innovative clinical development programs that shape the future of medicine

  • Gain exposure to global stakeholders, advanced research methodologies, and evolving therapeutic areas

  • Access continuous learning, leadership development, and career progression opportunities

  • Contribute to meaningful work that directly improves patient lives worldwide


Application Process
Interested candidates should apply online by submitting an updated CV and a motivational statement through the official careers portal.


Important Disclaimer
Novo Nordisk does not charge any fees or request financial transactions during the recruitment process. Applicants are advised to stay cautious of fraudulent job offers.


Equal Opportunity Statement
Novo Nordisk is committed to fostering an inclusive workplace and provides equal employment opportunities to all qualified applicants regardless of background.