Job Description
At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism.
Eli Lilly Cork is made up of a talented diverse team of over 2000 employees across 60 nationalities who deliver innovative solutions that add value across a variety of Business Service functions including Finance, Information Technology, Medical, Clinical Trials and more. Eli Lilly Cork offers a premium workspace across our campus in Little Island, complete with flexible hybrid working options, healthcare, pension and life assurance benefits, subsidised canteen, onsite gym, travel subsidies and on-site parking.
The purpose of the Clinical Delivery Trial Associate role is to support EMP (Exploratory Medicine & Pharmacology) and to serve as a technical and process expert in exploratory and biopharmaceutical clinical development and document management for clinical trials and business processes.
Primary Responsibilities
* Clinical Trial Support: Establish, maintain and archive compound-related files and trial-related files as required per procedures.
* Partner closely with Clinical Trial Project Manager and Program Lead to deliver clinical trials.
* Obtain or prepare relevant documentation necessary for a clinical trial based on GCP (Good Clinical Practice) or local regulations for Start-up, Maintenance and Close-out of the study.
* Assist in the planning, forecasting, and tracking of trial budgets, Purchase Orders, and invoices.
* Assist in performing assessments of potential vendors and investigator sites for exploratory and biopharmaceutics clinical development studies.
* Identify, communicate, and resolve issues.
* Understand FRAP (Financial Responsibility and Authorization Policy) and consult with teams regarding FRAP compliance.
* Populate internal systems to ensure accuracy of trial / site performance.
* Populate Trial Master Files and libraries for future reference.
* Provide feedback and shared learning for continuous improvement.
Minimum Qualification Requirements
* Bachelor’s Degree in a scientific or health-related field; or equivalent qualifications/experience (3 years pharmaceutical industry experience).
* Understanding of the overall clinical development paradigm and the importance of efficient site activation and maintenance.
* Strong self-management, analytical and organizational skills.
* Demonstrated problem-solving abilities.
Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form for further assistance. Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.
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