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Associate Director – Clinical Research Lead, Oncology
Location
United States
Posted
92 days ago
Salary
$115.5K - $204.6K / year
Seniority
Senior
Job Description
Associate Director – Clinical Research Lead, Oncology
Eli Lilly and Company
• The Clinical Research Lead (CRL) is a strategic, field-based scientific leader responsible for driving the execution of Lilly clinical trials through exceptional investigator engagement and site performance management • Accountable for the full spectrum of investigator engagement from identification and qualification through enrollment, and support database lock, and study closeout • Serve as a clinical trial scientific ambassador, ensuring investigators deeply understand protocol intent, scientific rationale, and patient eligibility requirements • Develop and sustain strategic, high-trust relationships with investigators that span trials and therapeutic areas • Influence enrollment by co-creating tailored recruitment strategies aligned with site capabilities, patient population realities, and study objectives • Proactively find opportunities to reach new patients, accelerate enrollment and increase impact at priority sites, including for example, novel site models, community-based research initiatives etc • Capture and elevate critical insights from sites to optimize feasibility, protocol design, and study conduct • Lead site-level strategy and risk planning to ensure strong and predictable enrollment and data delivery • Leverage performance metrics to anticipate issues, intervene decisively, and maintain momentum toward clinical milestones • Drive inspection readiness as a continuous discipline across sites • Collaborate across functions and with vendor partners to resolve operational barriers, ensuring delivery with speed and quality • Provide oversight and quality assurance for vendor monitoring, escalating risks proactively • Act as a key liaison between field teams, vendors, and investigators, ensuring alignment, shared purpose, and continuous knowledge transfer
Job Requirements
- 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
- Minimum 2 years of relevant clinical or deep therapeutic area experience in Oncology
- 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
- English fluency and proficiency in local language(s) as needed
Benefits
- 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)
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