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Clinical Research Physician - Metabolics (Orforglipron)

Lilly
Lilly
0-2 years
Not Disclosed
10 Jan. 8, 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
Category: Medical
Employment Type: Full-Time, Regular
Job ID: R-97994


About Lilly

Lilly is a global healthcare leader committed to uniting caring with discovery to improve lives worldwide. Headquartered in Indianapolis, Indiana, Lilly focuses on developing life-changing medicines, advancing disease management, and contributing to communities through philanthropy and volunteerism. At Lilly, we put people first and strive to make healthcare better for patients, providers, and payers globally.


Purpose of the Role

The Clinical Research Physician (CRP) plays a critical role in medical affairs, clinical development, and brand strategy. Leveraging medical expertise and scientific knowledge, the CRP supports the launch and commercialization of innovative therapies, ensuring patients, healthcare providers (HCPs), and payers receive accurate, timely, and meaningful information.

The CRP works collaboratively with global Development teams, Therapeutic Area Programs, Clinical Pharmacology, Translational Medicine, and other cross-functional stakeholders to support the full spectrum of drug development and clinical trials. The role involves strategic input into clinical planning, study implementation, safety reporting, medical education, external engagement, and regulatory interactions.


Key Responsibilities

Medical and Scientific Expertise

  • Provide clinical and medical expertise within the therapeutic area to support brand commercialization and medical strategies.

  • Maintain detailed, up-to-date knowledge of product data, clinical evidence, and competitor landscape.

  • Collaborate with pricing, reimbursement, access (PRA), Clinical Operations, Corporate Affairs, Legal, Marketing, and Medical Information teams.

  • Contribute to scientific publications, protocol reviews, study reports, and regulatory documents.

  • Support development and delivery of internal medical education and field training for MAPs, MSLs, and sales representatives.

Clinical Research and Trial Management

  • Implement and manage local clinical trial plans, including site selection, start-up, investigator interactions, and trial oversight.

  • Participate in global and regional clinical trial planning and ensure compliance with timelines, quality standards, and local regulations.

  • Facilitate data dissemination and reporting, supporting evidence-based decision-making for internal and external stakeholders.

External Relations and Medical Engagement

  • Engage with HCPs, advocacy groups, professional societies, and government agencies to communicate relevant clinical data.

  • Support advisory boards, symposia, medical meetings, and publication planning.

  • Ensure compliant interactions with external stakeholders in line with local regulations and company policies.

Compliance and Governance

  • Ensure all activities comply with Good Clinical Practices (GCPs), local regulations, and global medical standards.

  • Review and approve promotional and non-promotional materials in line with compliance guidelines.

  • Maintain inspection readiness and adhere to corporate quality standards.

Leadership and People Management

  • Provide guidance, mentorship, and performance management for Medical Affairs Professionals (MAPs) and Medical Science Liaisons (MSLs).

  • Support recruitment, diversity, and professional development initiatives.

  • Foster a culture of continuous learning and knowledge sharing within the medical team.


Qualifications & Experience

Education & Licensure:

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

  • Therapeutic area expertise in Metabolics or related domains highly desirable.

Experience:

  • Proven clinical or industry experience supporting medical affairs, clinical research, and commercialization activities.

  • Demonstrated ability to balance scientific and business priorities.

  • Experience in cross-functional collaboration, strategic planning, and stakeholder engagement.

Skills & Competencies:

  • Strong communication, presentation, and interpersonal skills.

  • Proven leadership and mentorship capabilities.

  • Ability to analyze and interpret clinical data, generate insights, and support evidence-based decisions.

  • Knowledge of GCP, FDA, ICH guidelines, and local regulatory requirements.

  • Capacity for domestic and international travel as required.

  • Fluent in English (spoken and written).

Personal Attributes:

  • Strong initiative, self-motivation, and problem-solving abilities.

  • Strategic thinker with excellent planning, prioritization, and organizational skills.

  • Collaborative, adaptable, and capable of working in matrixed and fast-paced environments.