Clinical Research Physician – Incretins
Location: Indianapolis, Indiana, USA
Category: Medical
Job Type: Full-Time, Regular
Job ID: R-88387
About Lilly
Lilly is a global healthcare leader headquartered in Indianapolis, dedicated to discovering and delivering life-changing medicines and improving patient care. The company values scientific innovation, patient-focused solutions, and strong ethical practices.
Role Purpose
The Clinical Research Physician – Incretins (Senior/Executive Director level) serves as a key medical leader within the Diabetes & Obesity Business Unit – Global Medical Affairs, responsible for:
Medical strategy for product launch & commercialization
Supporting clinical development across all phases
Enhancing customer (patients, HCPs, payers) experience
Ensuring scientific excellence and regulatory compliance
Driving medical support across incretin therapies and obesity treatment spectrum
Primary Responsibilities
1. Medical & Business Support
Contribute to medical strategy, patient journey mapping & product planning
Provide medical input for regulatory submissions (NDA/sNDA)
Support pricing, reimbursement, and access (PRA) activities
Lead scientific data dissemination through conferences, advisory boards & publications
Guide development of educational content and slide decks
Collaborate with global scientific experts & professional societies
Review & support medical information responses and media inquiries
Represent Lilly at congresses, booths, and external events
Lead real-world evidence (RWE), observational studies & phase 3b/4 trials
2. Clinical Planning & Trial Support
Collaborate with CRSs, clinical operations, statisticians & investigators
Develop clinical protocols & data collection tools
Support site training, startup and ongoing monitoring
Ensure compliance with GCP, ethical reviews & regulatory requirements
Review IIT proposals, publications & scientific materials
Monitor patient safety and adverse events in alignment with corporate policies
Contribute to global alignment of phase 3b/4 & early phase studies
3. Regulatory & Scientific Support
Stay updated on medical literature, competitive landscape & clinical trends
Provide scientific training to clinical teams
Act as clinical and protocol expert across functions
Participate in scientific congresses & external engagements
Support scientific content for labels, submissions, PRA tools and publications
4. General Responsibilities
Serve as a strong representative of patients and the Lilly brand
Maintain deep expertise in:
Diabetes & obesity pathophysiology
Clinical management
Medical affairs strategy
RWE, observational research, and early-phase data
Ensure compliance with global/ local medical, regulatory and quality standards
Minimum Qualification Requirements
Medical Doctor (MD)
Board eligible/certified in:
Endocrinology OR
Diabetology OR
Obesity Medicine
U.S. or LCME-approved equivalent foreign medical training
Clinical experience in diabetes or obesity
Preferred Qualifications
Prior pharmaceutical industry experience (medical affairs/clinical development)
Experience working on obesity disease state
Knowledge of drug development process
Strong leadership & cross-functional influence
Strong communication, teamwork & negotiation skills
Ability to travel domestically/internationally
Fluent in English (written & verbal)
Compensation & Benefits
Anticipated annual salary:
$198,000 – $336,600
Additional benefits include:
Annual company bonus
401(k) & pension plans
Medical, dental, vision, prescription coverage
Flexible spending accounts
Life insurance, PTO, wellness programs
Employee support networks (ERGs)
Inclusivity Commitment
Lilly is an Equal Employment Opportunity employer. No discrimination based on age, gender, race, disability, orientation, nationality, etc.
Workplace accommodations available upon request.
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