Job Title: Clinical Research Physician – Incretins
Location: Indianapolis, Indiana, USA
Category: Medical
Job Type: Full-Time, Regular
Job ID: R-88387
Company Overview
At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees work to discover and bring life-changing medicines to patients, improve disease management, and contribute to communities through philanthropy and volunteerism.
Job Purpose
The Clinical Research Physician is a key member of the Diabetes and Obesity Business Unit – Global Medical Affairs team. The role provides scientific and medical expertise to support launch, commercialization, and ongoing clinical activities for incretins and obesity-related products.
Key objectives include:
Enhancing customer experiences (patients, providers, payers).
Supporting product development across all clinical trial phases.
Ensuring compliance with local and international regulations, GCPs, and Lilly standards.
Primary Responsibilities
1. Business / Customer Support (Pre- and Post-Launch)
Support planning and execution of symposia, advisory boards, and HCP meetings.
Assist medical information associates in preparation and review of medical content.
Train medical personnel, including medical liaisons and health outcomes staff.
Prepare or review scientific responses to customer or media inquiries.
Support development of slide sets, abstracts, posters, manuscripts, and publications.
Build and maintain collaborations with scientific experts, thought leaders, and professional societies.
Provide congress support: answer questions, present data, participate in customer events.
Participate in real-world evidence, observational studies, and patient-reported outcome initiatives.
2. Clinical Planning
Collaborate with Clinical Research Scientists, statisticians, and investigators to develop study protocols and data collection requirements.
Assist in investigator selection and study start-up activities.
Ensure study compliance with regulatory approvals, ethical boards, and GCPs.
Provide scientific guidance and training to investigators and site personnel.
Monitor patient safety and adverse events according to corporate safety policies.
Contribute to global alignment of Phase 3b/4 studies and early-phase trials as applicable.
3. Regulatory Support Activities
Stay updated on clinical practice trends, competitor products, and therapeutic developments.
Critically review and evaluate medical literature relevant to the product.
Provide scientific training to clinical study teams.
Serve as a scientific consultant and protocol expert.
Participate in medical congresses and symposia to disseminate scientific knowledge.
4. General Responsibilities
Serve as an ambassador for patients and Lilly products.
Demonstrate deep understanding of diabetes, obesity, incretins, and related clinical management.
Lead medical planning, data dissemination, and communication strategies across clinical phases.
Minimum Qualification Requirements
Medical Doctor (MD) board eligible or certified in Endocrinology, Diabetology, or Obesity, or equivalent post-medical school clinical training.
U.S. trained physicians must achieve board eligibility or certification; non-U.S. trained physicians must meet LCME-approved medical school requirements.
Preferred Qualifications / Experience
Previous experience in pharmaceutical medical affairs or clinical development.
Clinical experience in Diabetes and Obesity disease states.
Knowledge of drug development processes.
Demonstrated ability to balance scientific and business priorities.
Strong cross-functional influence, leadership, and communication skills.
Ability to travel domestically and internationally as required.
Teamwork, organizational, and negotiation skills.
Fluent in English (verbal and written).
Compensation & Benefits
Anticipated salary: $198,000 – $336,600 (full-time equivalent).
Eligibility for company bonus based on individual and company performance.
Comprehensive benefits: 401(k), pension, medical, dental, vision, life insurance, vacation, leave of absence, flexible spending accounts, wellness programs, employee clubs, and fitness benefits.
Lilly reserves the right to amend compensation and benefits.
Equal Opportunity & Accessibility
Lilly is committed to inclusion and provides accommodations for individuals with disabilities.
To request accommodations during the application process, complete the workplace accommodation form.
Lilly is an equal opportunity employer and does not discriminate based on age, race, color, religion, gender, sexual orientation, gender identity/expression, genetic information, national origin, veteran status, disability, or any other legally protected status.
Employee Resource Groups (ERGs): Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network, Lilly India Network, Organization of Latinx at Lilly, PRIDE, Veterans Leadership Network, Women’s Initiative for Leading at Lilly, enAble.
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