Lilly
Senior Associate/Manager - Clinical Trial Project Management, Exploratory Medicine
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Eli Lilly Cork – Clinical Trial Project Manager (CTPM) Associate
At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world. Headquartered in Indianapolis, Indiana, our 50,000+ global employees tackle complex challenges to deliver life-changing medicines, strengthen health management, and support the communities we serve.
About Eli Lilly Cork
Eli Lilly Cork comprises a 2,000+ diverse team across 60 nationalities, delivering innovative solutions in finance, IT, medical, clinical trials, and more. Locations in Little Island offer:
- Premium workspace with flexible hybrid working
- Competitive benefits: healthcare, pension, life assurance, subsidised canteen, on-site gym, travel subsidies, and parking
- Holistic perks:
- In-house People Development & Educational Assistance
- ‘Live Your BEST Life’ wellbeing initiatives
Lilly Cork’s commitment to diversity, equity, and inclusion (DEI) ensures a welcoming environment. Our pillars include:
- EnAble: Accessibility for people with disabilities
- embRACE: Cultural & nationality inclusion
- LGBTQ+ & Ally Network
- Gender Inclusion Network (GIN)
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Overview: Clinical Trial Project Manager (CTPM) Associate
The CTPM Associate leads clinical trial teams, ensuring on-time, on-budget, and high-quality execution. Responsibilities include:
- Project management of local, regional, and global trials
- Risk & budget oversight
- Stakeholder coordination (CPM, regional teams, vendors)
- Regulatory compliance & process leadership
- Scientific advisory support
This role demands detail-oriented leadership, cross-functional collaboration, and resilience—because every day matters for patients.
Key Responsibilities
1. Project & Regional Operations
- Define and monitor trial scope, timelines, and budget
- Align global enrollment plans across geographies
- Assess trial-level risks and devise mitigation strategies
- Act as communications hub for cross-functional teams
- Resolve issues using critical thinking with vendors, affiliates, and global teams
2. Process & Regulatory Expertise
- Maintain Trial Master File (TMF) for compliance
- Anticipate challenges and propose proactive solutions
- Champion continuous improvement
- Solidify expertise in operational models, GCP, and worldwide regulations
3. Scientific Contribution
- Technical input for clinical/regulatory documents
- Prepare for regulatory agency meetings and response drafting
- Drive feasibility and trial design via scientific insights
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Minimum Qualifications
- Bachelor’s/Master's degree in a scientific or health-related field (preferred)
- 3+ years’ experience in clinical research
- Leading clinical trial projects preferred
Highly Desired Skills
- Proficiency in project management tools (e.g., ProChain, MS Excel)
- Cross-cultural influence ability
- Effective communication & problem-solving
Preferred Profiles
- Experience in exploratory clinical development or pharmaceutics
- Prior site-level or affiliate leadership
- International project collaboration
- Travel readiness (up to 10%)
Inclusion Commitment
Lilly promotes workplace accessibility. If you require accommodation during the application process, visit: https://careers.lilly.com/us/en/workplace-accommodation.
Lilly does not discriminate on age, race, religion, gender, sexual orientation, nationality, disability, or veteran status. Together, we deliver better lives for people around the world. Welcome to #WeAreLillyUKandIreland.
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