Intern-Clinical Development

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. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world.

Intern – Expert Specialist, Clinical Development (MCD)

The Intern – Expert Specialist (ES) provides technical and project administrative support to the Clinical Development Trial Lead (CDTL) and Clinical Development Organization 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).

Primary Responsibilities:

1. 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.

2. 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 CV 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. Lilly Net Collaboration Site; eTMF) and maintain project team rosters.

3. 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.

Note: The responsibilities list is not exhaustive, and tasks may vary depending on the business need or clinical trial/study allocation

Minimum Qualification Requirements:

• Master's degree in a scientific, health, communications, health outcomes, health economics, public health related field.

• Currently pursuing the undergraduate programs in life science from deemed universities, with desired merit.

• Excellent communication and interpersonal skills (both verbal and written)
• Demonstrate efficient learning agility

• Computer proficiency and experience using a variety of software packages (eg, MS word, Power point, Project, Excel)

Other Information/Additional Preferences:

• Previous training and experience in disseminating results in clinical, health economics, health outcomes, health literacy, disease management, and/or population health.

• Understanding in clinical development, clinical trial process, health-outcomes research, or regulatory activities.

• Clinical pharmacology, therapeutic area, health outcomes, or other medical and scientific specific knowledge and experience specific to hiring area (e.g., neuroscience, oncology, cardiovascular, immunology or endocrine expertise).

• Ability to communicate clearly and succinctly with all audiences and forums through exemplary oral and written communication skills.

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. 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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