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Clinical Research Physician - Metabolics (Orforglipron)

Lilly
Lilly
0-2 years
Not Disclosed
10 Jan. 9, 2026
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

Clinical Research Physician – Metabolics (Orforglipron)

Location: Gurgaon, Haryana, India
Job Type: Full-Time, Regular
Job ID: R-97994


About Lilly

At Lilly, we unite caring with discovery to make life better for people worldwide. As a global healthcare leader headquartered in Indianapolis, Indiana, our employees are committed to discovering and delivering life-changing medicines, advancing disease understanding, and giving back to communities through philanthropy and volunteerism. We prioritize patients and strive to make a meaningful impact on healthcare globally.


Purpose of the Role

The Clinical Research Physician (CRP) is an integral member of Lilly’s Medical Affairs, Development, and Brand Teams, providing medical and scientific expertise across product launch, commercialization, and clinical development activities. The CRP works closely with global Development, Therapeutic Area Programs, Early Phase/Clinical Pharmacology, and Translational Medicine teams to support strategic clinical planning, local trial execution, and scientific data dissemination.

The CRP also collaborates with cross-functional teams including Pricing, Reimbursement & Access (PRA), Regulatory, Medical Information, Global Product Safety, and Clinical Operations, ensuring alignment with global medical strategies and compliance with local and international regulations.


Key Responsibilities

Medical Expertise & Strategic Support

  • Provide therapeutic area expertise for assigned products and portfolios.

  • Develop and implement local clinical plans aligned with global/regional strategies.

  • Contribute to medical strategies supporting brand commercialization, pricing, and access.

  • Lead clinical data analyses, interpretation, and presentation for internal and external stakeholders.

  • Ensure scientific accuracy and compliance in promotional and non-promotional materials.

Clinical Research & Trial Execution

  • Participate in site selection, trial initiation, issue resolution, and monitoring of India clinical trials.

  • Support investigator engagement, advisory boards, and medical meetings.

  • Collaborate with Clinical Operations and Medical Affairs to ensure trial quality, speed, and value.

Scientific Communication & Education

  • Disseminate clinical and scientific data to HCPs, payers, and patient communities.

  • Provide training and mentorship to Medical Affairs Professionals (MAPs) and Medical Science Liaisons (MSLs).

  • Contribute to publications, slide decks, clinical reports, and medical letters.

  • Support internal and external scientific presentations, symposia, and advisory boards.

Compliance & External Relations

  • Ensure adherence to local laws, global regulations, Good Clinical Practices (GCP), and Lilly policies.

  • Maintain relationships with HCPs, advocacy groups, and professional societies.

  • Address external queries and participate in regulatory and Health Technology Assessment submissions.

Leadership & Team Development

  • Mentor and guide MAPs and MSLs on clinical knowledge, trial data, and field medical plans.

  • Support performance management, recruitment, and professional development initiatives.


Qualifications

Basic Requirements

  • Medical degree (MBBS/MD) with full Medical Council registration or eligibility.

  • Therapeutic area clinical or industry expertise within metabolics or related domains (highly desirable).

  • Strong communication, organizational, and leadership skills.

  • Ability to balance scientific priorities with business objectives.

  • Willingness to travel domestically and internationally as required.

  • Fluent in English (written and verbal).

Preferred Attributes

  • Demonstrated ability to develop partnerships with internal and external stakeholders.

  • Experience in clinical trial design, execution, and scientific data dissemination.

  • Understanding of regulatory submissions, HTAs, and commercial considerations in medical affairs.

  • Proven ability to mentor and guide team members and cross-functional colleagues.


Why Join Lilly

  • Be part of a global healthcare leader transforming patient care worldwide.

  • Work in a collaborative, innovative environment that values diversity, equity, and inclusion.

  • Engage in professional development, learning, and career growth opportunities.

  • Contribute directly to improving patient outcomes through scientific and medical expertise.

Lilly is committed to equal employment opportunities for all applicants. We actively support individuals with disabilities and provide accommodations throughout the hiring process.

For more information, please visit Lilly Careers – Workplace Accommodation.

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