Associate Director - Clinical Development Trial Lead (cdtl)

Eli Lilly UK

United Kingdom
Base: $115,500 - $169,400; bonus/equity: compyny b...
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Lead cross-functional study team
Develop and execute complex clinical trials
Manage trial scope, timeline, risk, and budget
** Eli Lilly is seeking an Associate Director - Clinical Development Trial Lead (CDTL) to lead cross-functional clinical trial teams, ensuring the execution of complex trials on time and within budget. The ideal candidate will have significant clinical research experience, strong project management skills, and a background in oncology. **

Job Summary

  • The Clinical Development Trial Lead (CDTL), Associate Director 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.
  • Independently drive and influence local, regional and global, cross-functional study team throughout study implementation, execution and closure empowering them to meet the clinical trial deliverables, including proactive issue management, contingency planning and issue resolution.
  • Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance).

Matching Summary

Match Score: 75

** Eli Lilly is seeking an Associate Director - Clinical Development Trial Lead (CDTL) to lead cross-functional clinical trial teams, ensuring the execution of complex trials on time and within budget. The ideal candidate will have significant clinical research experience, strong project management skills, and a background in oncology. **

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 and execution
  • Uphold GCP and Lilly standards

Nice-to-have

  • Influence without authority
  • Embrace strategic organizational changes
  • Solution-oriented approach
  • Continuous improvement activities

Key Requirements

  • 5 years clinical research experience
  • Bachelors or University degree
  • Oncology background preferred
  • Prior clinical trial site-level or affiliate experience preferred

Work Rights

Not specified

Tailored Resume

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