Global Clinical Trial Project Manager (Associate)

Eli Lilly and Company

Cork

Hybrid

EUR 70,000 - 90,000

Full time

14 days+
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Benefits offered by this job

Healthcare
Pension
Life assurance
Hybrid work

Job summary

Eli Lilly Cork is seeking a Clinical Trial Project Manager Associate to lead cross-functional teams in the development and execution of clinical trials, delivering quality results on time and within budget. The role requires strong project management and regional/regional operational knowledge.

You will collaborate with multiple functions, manage risks, and coordinate training and oversight of trial activities to ensure compliance and success of global studies.

Qualifications

  • Bachelor's degree in a scientific or health-related field is required or an advanced degree.
  • Minimum of 3 years clinical trial experience or relevant experience in clinical research.
  • Experience leading cross-functional study teams and coordinating regional/global trials.

Responsibilities

  • Lead cross-functional study teams to develop and execute clinical trials regionally and globally.
  • Coordinate enrollment plans, timelines, risks, and budgets for trials.
  • Ensure Trial Master File is complete, inspection-ready, and aligned with regulatory requirements.
  • Provide scientific and regulatory input for study documents and regulatory interactions.

Skills

Project management
Cross-functional collaboration
Leadership
Communication
Problem solving

Education

Bachelor's degree in scientific or health-related field
3 years clinical research experience or related field

Tools

MS Project
MS Excel
MS PowerPoint
Critical Chain
ProChain Enterprise

Job description

Eli Lilly Cork is seeking a Clinical Trial Project Manager Associate to lead cross-functional teams in the development and execution of clinical trials, delivering quality results on time and within budget. The role requires strong project management and regional/regional operational knowledge.

You will collaborate with multiple functions, manage risks, and coordinate training and oversight of trial activities to ensure compliance and success of global studies.

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