Job Title: Clinical Research Physician – Metabolics (Orforglipron)
Category: Medical Affairs / Clinical Research
Location: Gurgaon, Haryana, India
Job Type: Full-Time, Regular
Experience Required: 3–7 Years
Job ID: R-97994
About Lilly
At Lilly, we unite caring with discovery to improve lives worldwide. As a global healthcare leader headquartered in Indianapolis, Indiana, we are committed to discovering and delivering life-changing medicines, advancing disease understanding and management, and giving back to communities through philanthropy and volunteerism. We value innovation, collaboration, and a patient-first mindset.
Purpose of the Role
The Clinical Research Physician (CRP) – Metabolics (Orforglipron) will serve as a key medical and scientific leader, integrating clinical expertise, research knowledge, and strategic planning to support launch, commercialization, and clinical development activities. This role ensures the delivery of scientifically accurate, compliant, and high-impact medical initiatives that enhance the patient and healthcare professional (HCP) experience.
The CRP will also collaborate with global development teams, therapeutic area programs, early-phase clinical pharmacology, translational medicine, and medical affairs teams, contributing across the full spectrum of drug development, clinical trials, and medical communication initiatives.
Key Responsibilities
Medical Expertise & Scientific Leadership
Serve as a subject matter expert in metabolic therapeutics, providing insights for brand and clinical strategy
Maintain detailed, current knowledge of the molecule(s) and relevant clinical data
Contribute to medical education, publications, clinical trial reporting, and internal/external presentations
Support regulatory submissions, health technology assessments (HTAs), and scientific communications
Clinical Trial & Research Support
Implement global and regional clinical trial plans locally with adherence to GCP, ICH guidelines, and Lilly policies
Participate in site selection, trial initiation, issue resolution, and investigator interactions
Lead medical monitoring and ensure patient safety, protocol compliance, and data integrity
Stakeholder Engagement
Build effective partnerships with clinicians, Key Opinion Leaders (KOLs), advocacy groups, and external professional bodies
Support internal teams (MSLs, MAPs, sales, medical affairs) through scientific training and guidance
Provide strategic input to commercial, pricing, reimbursement, and access (PRA) activities
Medical Communication & Publications
Develop, review, and approve promotional and non-promotional materials ensuring compliance with regulations
Lead scientific content creation for presentations, slide decks, and advisory boards
Drive dissemination of clinical data and insights to internal teams and external stakeholders
Team Leadership & Mentorship
Provide guidance and coaching to direct reports, including Medical Affairs Professionals (MAPs) and Medical Science Liaisons (MSLs)
Participate in recruitment, performance management, and professional development of team members
Qualifications & Requirements
Education & Professional Credentials
MBBS/MD with full medical council registration or eligibility
Minimum 3–7 years of clinical practice or industry experience in metabolic therapeutics, endocrinology, or related areas
Skills & Competencies
Strong clinical and scientific knowledge with expertise in metabolic disorders
Demonstrated ability to balance scientific priorities with business objectives
Excellent written and verbal communication, presentation, and interpersonal skills
Strong project management, organizational, and analytical abilities
Leadership skills with the ability to mentor and develop team members
Willingness to travel domestically and internationally as required
Desirable Experience
Exposure to clinical trials, drug development, and medical affairs in the pharmaceutical industry
Knowledge of regulatory, pricing, reimbursement, and access frameworks
Why Join Lilly
Contribute to innovative metabolic therapies and impactful patient solutions
Collaborate with global experts and gain exposure to international clinical development programs
Work in a culture that values diversity, equity, inclusion, and professional growth
Access opportunities for skill development, mentorship, and cross-functional leadership
Lilly is committed to equal opportunity employment and supports individuals with disabilities. For accommodation during the application process, please complete the accommodation request form.
Apply Now: Submit your CV and cover letter online via the Lilly careers portal.
Application Deadline: Open until the position is filled
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