Clinical Research Physician – Incretins
Location: Indianapolis, Indiana, USA
Category: Medical
Job Type: Full-Time, Regular
Job ID: R-64932
About the Role
Lilly is a global leader in scientific innovation and patient-focused healthcare. As part of the Diabetes and Obesity Business Unit within Global Medical Affairs, the Clinical Research Physician – Incretins plays a critical role in advancing clinical development, supporting product launches, and ensuring scientific leadership across the therapeutic area.
This position supports multidisciplinary teams by providing medical expertise across clinical development, real-world evidence generation, regulatory interactions, scientific communication, and global medical strategy.
Position Overview
The Clinical Research Physician contributes medical and scientific leadership across the full spectrum of drug development, including Phase I–IV clinical trials, clinical planning, safety assessment, and post-marketing activities. This role supports global and regional medical plans, clinical operations, external expert engagement, and cross-functional collaboration to enhance product strategy for incretin therapies and obesity management.
Key Responsibilities
Medical Affairs & Scientific Leadership
Provide expert medical support for product launches, commercialization, and life-cycle management.
Lead development of scientific content, data communication strategies, and medical education materials.
Support regulatory submissions, labeling updates, and interactions with global regulatory agencies.
Contribute to pricing, reimbursement, and access (PRA) strategies by supplying robust clinical and medical insights.
Engage with thought leaders, healthcare professionals, and professional societies to ensure scientific alignment.
Clinical Research & Development
Collaborate with Clinical Research Scientists, statisticians, health outcomes teams, and investigators on protocol design and study execution.
Support identification and selection of clinical investigators.
Ensure compliance with GCP, global regulations, and corporate safety standards.
Monitor patient safety, adverse events, and study integrity throughout clinical trials.
Review investigator-initiated trial (IIT) proposals, publications, and global clinical study plans.
Scientific Data Dissemination
Lead and participate in congress presentations, advisory boards, and scientific symposia.
Support development of abstracts, posters, manuscripts, and data presentations.
Contribute to real-world evidence, observational studies, and patient-reported outcomes to enhance clinical insights and commercial strategy.
Business & Customer Support
Support symposia, advisory boards, and medical education initiatives.
Provide scientific responses to medical information inquiries from healthcare professionals and media.
Train medical teams, field medical personnel, and health outcomes staff.
Collaborate with external experts to maintain scientific credibility and medical engagement.
General Responsibilities
Represent the company as a scientific ambassador to patients, providers, and partners.
Stay updated on competitive intelligence, scientific advances, and disease-area developments.
Demonstrate leadership in cross-functional collaboration, medical training, and team development.
Minimum Qualification Requirements
Medical Doctor (MD) degree.
Board eligible or board certified in Endocrinology, Diabetology, or comparable clinical specialty.
Non-U.S. trained physicians must meet LCME-equivalent medical school requirements.
U.S.-based roles require eligibility to work in the United States.
Experience Required
Clinical experience in Diabetes care and strong understanding of diabetes and obesity pathophysiology.
Previous industry experience in pharmaceutical medical affairs or clinical development (highly preferred).
Experience supporting clinical trials, medical strategy, or scientific communication.
Knowledge of drug development processes and regulatory pathways.
Demonstrated leadership, collaboration, and communication capabilities across global teams.
Ability to travel domestically and internationally as needed.
Preferred Qualifications
Experience in obesity disease state or incretin therapies.
Experience generating and interpreting real-world evidence.
Strong scientific writing, data interpretation, and presentation skills.
Ability to balance scientific integrity with business needs.
Fluent in English, both written and spoken.
Compensation & Benefits
Estimated annual compensation: $198,000 – $330,000, based on experience, qualifications, and geographic factors.
Eligible employees may also receive:
Annual performance bonus
401(k) and pension participation
Health, dental, vision, and prescription benefits
Life insurance and disability benefits
Paid time off and leave programs
Flexible spending accounts
Well-being and employee assistance programs
Equal Opportunity Statement
Lilly is an Equal Opportunity Employer committed to a diverse and inclusive workplace. All qualified applicants will receive consideration without regard to race, color, gender, sexual orientation, national origin, disability, veteran status, or any protected characteristic. Reasonable accommodations are available upon request during the application process.
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Siliguri |Illinois :
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Kyiv |Lima Region :
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South Africa | Midrand |Nišava District :
Niš |Bohemia :
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