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Associate Director, Clinical Research Lead – East Coast/Midwest
Eli Lilly and CompanyClinical Research Lead driving execution of Lilly clinical trials through investigator engagement. Ensuring trials are prioritized at high-performing sites, with quality, speed, and insight.
Posted 5/28/2026full-timeChicago • Illinois, North Carolina • 🇺🇸 United StatesSenior💰 $115,500 - $204,600 per yearWebsite
Tech Stack
Tools & technologiesGoogle Cloud Platform
About the role
Key responsibilities & impact- Drive the execution of Lilly clinical trials through exceptional investigator engagement and site performance management
- Ensure Lilly’s portfolio is prioritized at high-performing sites and that trials are delivered with quality, speed, and insight
- Combine deep therapeutic and scientific knowledge with strategic agility to influence investigators, elevate protocol understanding, and co-develop tailored enrollment strategies
- Serve as trusted partners to investigators, building strong relationships that improve return on enrollment
- Partner closely with internal Lilly teams to ensure that insights from the field shape development strategies
- Lead site-level strategy and risk planning to ensure predictable enrollment and data delivery
Requirements
What you’ll need- Bachelor’s degree or equivalent; strong preference for scientific, clinical, or health-related fields
- Minimum 5 years of experience in clinical research or pharmaceutical industry with experience directly interacting with or working with HCPs and clinical sites
- Advanced degree in a scientific or clinical field (PharmD, PhD, MD, or MSc preferred)
- Experience in the Neurodegeneration, Immunology or Cardiometabolic Health therapeutic spaces
- Excellent understanding of GCP, clinical development and operations, and trial lifecycle
- Demonstrated understanding of the therapeutic landscape and standards of care, with the ability to apply this knowledge to decision making
- Proven ability to build credibility and influence HCP community through scientific acumen and relationship strength
- Strategic approach with demonstrated success in delivering results in complex, fast-paced environments
- Data-driven decision-making skills; ability to interpret and act on performance and operational metrics
- Excellent communication, negotiation, and organizational skills
- Deep therapeutic area knowledge and familiarity with local clinical research ecosystems
- Experience directly influencing clinical site performance and driving enrollment success
- Track record of delivering or exceeding performance targets in a collaborative matrix environment
- Experience working with regulators or national bodies in support of clinical trial delivery
- English fluency and proficiency in local language(s) as needed
Benefits
Comp & perks- eligibility to participate in a company-sponsored 401(k)
- pension
- 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)
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
clinical researchGCPclinical developmenttrial lifecycledata-driven decision-makingperformance metricsNeurodegenerationImmunologyCardiometabolic Healthscientific acumen
Soft Skills
communicationnegotiationorganizational skillsrelationship buildingstrategic approachinfluencecredibilitycollaborationadaptabilityproblem-solving
Certifications
Bachelor’s degreePharmDPhDMDMSc