Amgen is looking to develop and execute regulatory policies of global and regional importance that impact Amgen's business, specifically in the areas of Oncology, Inflammation, General Medicine, and Rare Disease, to serve patients living with serious illnesses.
Requirements
- Strong computer skills including experience with MS Office, Smartsheet, and SharePoint.
- The use of ChatGPT and Co-pilot to support research preferred.
- Master's degree in regulatory affairs or life sciences.
- Strong interpersonal, problem solving, and conflict resolution skills.
- Excellent organizational, process and project management skills.
Responsibilities
- Investigate policy research questions on key policy topics and determine the implications of emerging regulatory developments.
- Analyze regulatory guidances and other regulatory policy documents to inform policy strategies and positions.
- Support the development of Amgen regulatory policy positions and strategies.
- Prepare presentations and other communications to support alignment on positions and strategies across the Amgen organizations and regions.
- Support external engagement with industry partners and regulators.
- Partner with policy leads to develop whitepapers, policy analysis documents, and advocacy materials on priority policy issues.
- Plan and help manage projects for agreed upon policy objectives under the direction of in partnership with policy lead(s).
Other
- 18 years or older
- Graduated with a bachelor's degree from an accredited college or university
- Currently enrolled in an MBA program for an MBA internship OR a Master's program for a Master's internship OR a PharmD program for a PharmD internship OR Ph.D. for a PhD internship from an accredited college or university
- Must not be employed at the time the internship starts
- Student must be located in the United States for the duration of the Intern
