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Eli Lilly is seeking an Associate Director, Clinical Development Trial Lead (CDTL) to lead and manage complex clinical trials, ensuring they meet quality, timeline, and budget goals. The ideal candidate should have a strong background in clinical research, project management, and leadership skills to effectively coordinate cross-functional teams.
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Job Summary
Independently leads the cross-functional study team in the development and execution of complex clinical trials and is accountable both regionally and globally to deliver clinical milestones on trial(s) with quality, on time, and within scope and budget.
Partner with other organizations to coordinate and participate in Investigator Study Specific Training (ISSTs)/ Affiliate Study Training (ASTs).
Leverage expertise to make timely decisions for ambiguous and complex situations.
Matching Summary
Match Score: 75
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Eli Lilly is seeking an Associate Director, Clinical Development Trial Lead (CDTL) to lead and manage complex clinical trials, ensuring they meet quality, timeline, and budget goals. The ideal candidate should have a strong background in clinical research, project management, and leadership skills to effectively coordinate cross-functional teams.
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Salary
Base: $115,500 - $169,400; Bonus/Equity: company bonus; Benefits: comprehensive benefit program
Skills & Requirements
Must-have
lead cross-functional study team
develop and execute complex clinical trials
manage trial scope, timeline, risk, and budget
drive study implementation, execution, and closure
manage TPO qualification, selection, and oversight
ensure trial master file is inspection ready
leverage scientific and regulatory knowledge
Nice-to-have
demonstrate independent leadership
influence without authority
proactive issue management and resolution
continuous improvement activities
act as a coach for peers and new CDTLs
Key Requirements
Bachelors or University degree
5 years clinical research experience
Applied knowledge of project management methodology
Demonstrated ability to lead and work effectively cross-culturally
Prior clinical trial site-level or affiliate experience