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Eli Lilly and Company

Clinical Design Physician, Neuroscience

Eli Lilly and Company

Clinical Design Physician designing Phase II to IV clinical programs in neuroscience at Lilly. Delivering life-changing medicines and strengthening health management in a collaborative environment.

Posted 7/28/2026full-timeIndianapolis • 🇺🇸 United StatesMid-LevelSenior💰 $198,000 - $356,400 per yearWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in designing Phase II to Phase IV clinical programs within the neuroscience therapeutic area, with a strong foundation in statistical science and a deep understanding of therapeutic area pathology and treatment standards. Proven ability to collaborate with clinical research teams and engage with external experts to inform clinical trial design and strategy.

Highest-signal resume keywords
Medical Doctor or Doctor of OsteopathyBoard Certification or Eligibility in NeurosciencePharmaceutical Industry ExperienceStatistical Science ExpertiseGlobal Clinical Trial Design Experience

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Clinical Trial DesignNeuroscience Therapeutic Area KnowledgeBayesian StatisticsStudy Protocol DevelopmentClinical Research Collaboration
Soft Skills
Strong Communication SkillsRelationship BuildingCollaboration
Certifications & Qualifications
Board Certification or Eligibility
Industry Keywords
Phase II to Phase IV StudiesClinical DevelopmentTherapeutic Area PathologyPathophysiologyInvestigator Identification

About the role

Key responsibilities & impact
  • Design Phase II to Phase IV clinical programs and studies within the neuroscience therapeutic area.
  • Translate therapeutic area and asset team strategy into clear objectives and associated clinical development program and trial optionality.
  • Represent program and trial design optionality to asset teams and Sr. Leaders to inform prioritization of an option that will be translated into clinical protocol(s).
  • Bring the medical/clinical perspective to the Design Team to inform the design of study protocols.
  • Collaborate with clinical research staff in the design and conduct of clinical trials.
  • Support investigator identification and selection, in conjunction with Clinical Development.
  • Establish and maintain collaborations and relationships with external experts, thought leaders, and the general medical community.
  • Engage appropriately with asset and development teams on relevant external activities.

Requirements

What you’ll need
  • Medical Doctor or Doctor of Osteopathy.
  • Board eligible or certified in relevant field or have completed comparable level of post-medical school clinical training relevant to the country of hiring.
  • US trained physicians must have achieved board eligibility or certification.
  • Pharmaceutical Industry experience or research experience of at least three (3) years relevant to clinical trial design of PhII to Phase IV studies.
  • Board certification or eligibility within Neuroscience or related area strongly preferred.
  • Strong understanding of therapeutic area pathology, pathophysiology, unmet needs, and treatment standards in major geographies.
  • Strong foundation in statistical science, including Bayesian statistics, as applied to study design.
  • Global / multi-national design or development experience.
  • Willing to relocate to Indianapolis.
  • Fluent in English, with strong communication skills, verbal and written.

Benefits

Comp & perks
  • Comprehensive benefit program
  • Eligibility to participate in a company-sponsored 401(k)
  • Pension benefits
  • Vacation benefits
  • Eligibility for medical, dental, vision and prescription drug benefits
  • Flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts)
  • Life insurance and death benefits
  • Certain time off and leave of absence benefits
  • Well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities)