Expert Specialist - Clinical Development

Eli Lilly Eli Lilly · Pharma · Cork, Ireland

This role provides technical and project administrative support for clinical trial execution at Eli Lilly. Responsibilities include managing study budgets, ordering and tracking supplies, tracking enrollment data, maintaining study files and documentation for regulatory inspections and submissions, and managing clinical trial systems by inputting and updating study timelines and generating reports. The role requires a two-year degree or equivalent experience and proficiency in various software packages.

What you'd actually do

  1. Assist in the management of study budgets including the setup of purchase orders and e-requisitions
  2. Order, track, and ship study supplies, tools, and/or instruments
  3. Track and report Regional/Global enrollment data for ongoing clinical studies
  4. Support and partner with CDTLs and Management to oversee maintenance and inspection readiness of study files (e.g. eTMF, study collaboration sites, etc.) including quality reviews (routine and pre-inspection), associated updates, and indexing
  5. Accurately input study timelines and other trial level required fields into clinical trial database, monitors and updates fields as study timelines or other information changes and troubleshoots illogical data.

Skills

Required

  • Two-year degree or 2 years administrative or technical experience
  • Computer proficiency and experience using a variety of software packages (e.g., Microsoft Word, Excel, Power Point, Project)

Nice to have

  • Strong communication skills; able to communicate clearly and succinctly with team members and leadership
  • Demonstrated ability to work effectively cross-culturally as well as across regions/geographies with strong customer service skills
  • Strong teamwork and interpersonal skills including demonstrated ability to flex to changing business needs, attention to detail, strong self-management, organizational skills