Senior Pharmacoepidemiology Project Lead

Eli Lilly and Company; Cork; Hybrid; EUR 72,000 - 106,000; Full time

Benefits offered by this job

Healthcare

Pension

Life assurance

Canteen subsidy

On-site gym

Travel subsidies

On-site parking

Educational assistance

Wellbeing programs

Job summary

Lilly Cork is seeking a Clinical Development Project Manager (PEPM), Associate Director/Director, to lead a cross-functional team across regionally and globally.

You will drive planning, execution and delivery of complex pharmacoepidemiology studies, ensure alignment with regulatory needs, and manage risks, budgets and stakeholder communications while advancing trials to milestones with quality and efficiency.

Qualifications

• Bachelor's degree or higher in a scientific/health field; 5+ years clinical research experience.
• Experience leading cross-functional clinical trials and program management.
• Strong knowledge of GCP and regulatory requirements.
• Ability to coach peers and lead through change.
• Willingness to travel periodically.

Responsibilities

• Lead planning, execution and delivery of a diverse pharmacoepidemiology study portfolio.
• Provide strategic input on study design and data source selection.
• Ensure alignment with regulatory requirements, product safety needs and business objectives.
• Collaborate with CROs and internal teams; manage budgets and resources.
• Drive risk mitigation and contingency planning across studies.

Skills

Project management

Cross-cultural leadership

Coaching others

Strategic adaptability

Influence without authority

Cross-functional collaboration

Communication skills

Problem solving

Navigating ambiguity

Education

Bachelor's or University degree in science/health

Advanced degree in related field

Tools

Veeva

MS Project

MS Excel

MS PowerPoint

PowerBI

Job description

Lilly Cork is seeking a Clinical Development Project Manager (PEPM), Associate Director/Director, to lead a cross-functional team across regionally and globally.

You will drive planning, execution and delivery of complex pharmacoepidemiology studies, ensure alignment with regulatory needs, and manage risks, budgets and stakeholder communications while advancing trials to milestones with quality and efficiency.