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Eli Lilly and Company is a multinational pharmaceutical and healthcare company focused on discovering, developing, manufacturing, and commercializing prescription medicines. Its work spans therapeutic areas including diabetes, oncology, immunology, neuroscience, and pain, combining research and development with clinical trials, regulatory processes, biologic and small-molecule drug production, and global distribution.
Clinical Design Physician, Neuroscience (Hybrid)
Lead Phase II–IV neuroscience trial design for Eli Lilly and Company, shaping clinical strategy, protocols, and study execution. Partner with cross-functional teams and senior leaders to advance clinical development programs.
Description
- Design Phase II–IV neuroscience clinical programs and studies
- Convert therapeutic-area and asset-team strategies into development programs and trial alternatives
- Present program and trial design recommendations to asset teams and senior leaders
- Provide medical and clinical guidance on protocols in partnership with cross-functional teams
- Evaluate protocol features for feasibility, value, patient and investigator burden, and execution efficiency
- Contribute to asset strategy, portfolio clinical strategy, and asset-specific clinical plans
- Partner with clinical research staff on trial design and conduct, including sample sizes, timelines, grants, and governance reviews
- Assess study risks and support appropriate risk communication to participants
- Support investigator selection, participant recruitment and retention, and the handoff from design to execution
- Build and sustain relationships with external experts, thought leaders, professional societies, conferences, consortia, and the broader medical community
- Support scientific data dissemination, final reports, publications, and clinical design science
- Monitor medical literature, competing products, and scientific advances
- Identify and share effective practices for program and protocol design
- Help advance Lilly’s standards, tools, processes, templates, and design practices
Requirements
- MD or DO degree
- Board eligibility or certification in a relevant field, or comparable post-medical-school clinical training appropriate to the hiring country
- US-trained physicians must hold board eligibility or certification
- Physicians trained outside the US must have completed education and training at a medical school meeting LCME requirements
- At least three years of relevant pharmaceutical-industry or research experience in Phase II–IV clinical trial design
- Clinical research experience in neuroscience is preferred
- Strong knowledge of therapeutic-area pathology, pathophysiology, unmet needs, and treatment standards across major geographies
- Solid grounding in statistical science, including Bayesian methods applied to study design
- Experience with global or multinational study design or development
- Willingness to relocate to Indianapolis or demonstrate effectiveness in a hybrid work environment
- Willingness to travel for business-critical events, including limited domestic and international travel
- Fluency in English
- Excellent verbal and written communication skills
- Strong interpersonal, organizational, and negotiation abilities
- Ability to influence stakeholders across functions and within the discipline
- Regular experience using AI to accelerate deliverables
Benefits
- Company bonus tied in part to company and individual performance
- Company-sponsored 401(k) plan
- Pension plan
- Vacation benefits
- Medical, dental, vision, and prescription drug coverage
- Healthcare and dependent-care flexible spending accounts
- Life insurance and death benefits
- Eligible time-off and leave benefits
- Employee assistance program
- Fitness benefits
- Employee clubs and activities
- Disability accommodation support during the application process
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