Operational Excellence Leader

2 weeks ago

Cork, Cork, Ireland beBeeClinicalManager Full time €100,000 - €160,000
Job Description

Eli Lilly is a global healthcare leader that unites caring with discovery to make life better for people around the world.

We are committed to delivering innovative solutions that add value across various business functions, including finance, information technology, medical, and clinical trials.

Our team in Cork offers a premium workspace with flexible hybrid working options, healthcare, pension, and life assurance benefits, subsidised canteen, onsite gym, travel subsidies, and on-site parking.

We cater to all dimensions, ensuring inclusion of all ethnicities, nationalities, cultural backgrounds, generations, sexuality, visible and invisible disabilities, and gender.

We are committed to diversity, equity, and inclusion, with four pillars: EnAble, embRACE, LGBTQ+ & Ally, and GIN-Gender Inclusion Network.

Come join our diverse team – Be Creative, Be an Innovator, and most of all, Be Yourself.

Job Summary

The Trial Capabilities Manager leads and manages the daily operation of the clinical trial capabilities team in support of clinical development.

The Manager is accountable for ensuring accurate planning, prioritization across teams, and timely execution, working closely with site engagement at affiliates and across the trial capabilities teams.

The scope of work includes activities related to investigator sites readiness, maintenance, and close-out, ensuring country-specific requirements are met.

The manager ensures inspection readiness through a complete, accurate, and readily available Trial Master File.

  • Accountable for meeting and exceeding goals for clinical trial budgets and contracts operations for development programs.
  • Ensure compliance with local/regional requirements, data privacy requirements, and Lilly quality standards.
  • Manage communications/relationships and serve as the point of contact for the trial capabilities budgets and contracts team deliverables during site initiation, maintenance, and close-out, representing progress to business partners.
  • Accountable for daily prioritisation of work to meet business needs.
  • Provides expertise in conducting clinical research and keeping up-to-date with country/regional regulatory requirements.
  • Develop and streamline processes ensuring efficiency and improved productivity as well as meeting customer requirements.
  • Ensure inspection readiness through a complete, accurate, and readily available Trial Master File.

Clinical Trial Capabilities Responsibilities:

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