Scientific data and information are core assets of Lilly. Providing balanced, objective, and accurate information to regulators, the scientific community, health care professionals, payers, and patients in a consistent and timely fashion across the entire drug development lifecycle is fundamental to Lilly
The purpose of an Intern role is to learn and support teams across GSC
Primary Responsibilities: This job description is intended to provide a general overview of the job requirements at the time it was prepared. The job requirements of any position may change over time and may include additional responsibilities not specifically described in the job description. Consult with your supervision regarding your actual job responsibilities and any related duties that may be required for the position.
- Learn and support data integrity, scientific editing, encoring, clinical trial registry, Document Preparation, Development and Finalization/Document Management
- Learn the process of coordinating planning (including organizing/preparing outlines), writing (including first-draft authoring),
editing, reviewing and completing disclosures in GSC
- documents.
- Learn coordinate quality checks for accuracy,
- Learn processes across sub-functions and learn effective project management skills to support team members on disclosures across GSC
- Learn to build/communicate credible writing project timelines.
- Learn ways of effective communication on project status to stakeholders.
- Learn therapeutic area knowledge including disease state and compound(s) for assigned project(s).
- learn to enhance scientific communication skills to align with audience needs and technology/digital evolution.
- Exhibit flexibility in moving across document types, therapeutic areas, and compounds, depending on project assignment.
- Learn and enhance knowledge of guidelines applicable across GSC
- Gain technical expertise in specific document development.
- Network with others (including other function