Intern - Expert Specialist - Clinical Development

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, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work-but it's work worth doing. If you're driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us.

Intern - Expert Specialist - Clinical Development

Positions: 3

Start date: March 2027

Duration: 6 months

Salary: €30,500

Location: Lilly GBS, Little Island Cork

Type: Hybrid role requiring the successful candidate to be on site 50% of the month in Little Island, Cork and 50% working remotely.

Course Eligibility: BSC in Sciences, Health or similar in MTU

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. Inhouse People Development services, Educational Assistance, and our 'Live Your BEST Life' wellbeing initiatives are just some of the holistic benefits that enhance the career experience for our colleagues.

Eli Lilly Cork is committed to diversity, equity and inclusion (DEI). We cater for all dimensions ensuring inclusion of all ethnicities, nationalities, cultural backgrounds, generations, sexuality, visible and invisible disabilities and gender, with four pillars: EnAble, embRACE, LGBTQ+ & Ally and GIN-Gender Inclusion Network. EnAble, our pillar for people with disabilities and those that care for them, partners with the Access Lilly initiative to make our physical and digital environment accessible and inclusive for all. Together they are committed to promoting awareness to create a disability confident culture both at Eli Lilly Cork and beyond.

Come join our team - Be Creative, Be an Innovator, and most of all, Be Yourself!

Purpose of team and role

The Intern - Clinical Development Assistant provides technical and project administrative support to the Clinical Development Trial Lead (CDTL) and Clinical Development Organization (CDO) leadership to help enable on-time and on-budget delivery of key tasks during clinical trial execution. The Intern ES supports trial, asset, and portfolio level tasks that may be assigned to a specific asset team(s) or centrally across a Therapeutic Area (TA)/Business Unit (BU).

Responsibilities:

Clinical Trial Execution

• Order, track, and ship study supplies, tools, and/or instruments

• Participate in shared learning forums and may assist in coordination of regional and trial project-related meetings.

• Assisting in coordination of regional and trial project-related meetings.

Clinical Trial/Submission Documentation

• Support collection and review of clinical-trial related documents to support submission activities or other appropriate trial level activities like filing and archiving filing and archiving processes (i.e. collecting and verifying accurate information for financial disclosures/1572 and CVs, structure of newsletters, uploading minutes to the study collaboration site(s) or eTMFs as appropriate, etc.)

• Establish, maintain and use appropriate team information repositories (e.g. LillyNet Collaboration Site; eTMF) and maintain project team rosters.

Clinical Trial Systems Management

• Work with multiple systems like Veeva Vault, DrugDev, Hibbert, eCTS, Firecrest, Investigator Space, IWRS, Power BI, SIP, etc. to accurately input study timelines and other trial level required fields, monitors and updates fields as study timelines or other information changes, troubleshoots illogical data and assist in producing and distributing project status reports.

• Coordinate with CDTLs and Clinical Development Managers to generate regional-level, trial-level and compound-level milestone and budget reports, Veeva Vault accuracy and completeness reports, staff capacity reports, and other reports as needed.

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 (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

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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