Global Patient Safety and Regulatory Fellow with Butler, Regeneron, and the FDA
Butler University
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- Location
- Indianapolis, IN
- Job type
- Full time
- Posted
- Oct 30
- 1 day ago
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Career path
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About the company
Butler University
Higher education · 1,001 to 5,000 employees
What you'll do
- Examine career options within academic, pharmaceutical industry, medical, and regulatory environments.
- Demonstrate an understanding of the key elements of an academic environment and faculty roles within it.
- Explore various medical and regulatory components of pharmaceutical development and innovation.
- Develop an understanding of regulations and patient safety considerations regarding medication use.
- Construct expertise in patient and medication safety, focusing on tools and methods to make healthcare safer.
- Demonstrate personal, interpersonal, and teamwork skills critical for effective leadership.
- Focus on regulatory approaches in addressing risk management and medication error related issues associated with currently marketed drug and biologic products.
- Contribute to advancing the science of risk management and medication error prevention and analysis.
- Develop and understanding of pharmaceutical risk management tools available to assess and mitigate the risks of drug and biologic products.
- Enhance scientific writing skills.
- Engage at scientific conferences to network with other professionals in industry.
- Letter of intentPlease address to:Veronica Vernon, PharmD, BCPS, BCACP, MSCP, FAphAAssociate Professor and Chair of Pharmacy PracticeButler University College of Health ProfessionsIndianapolis, IN, USA
- Curriculum vitae
- Two letters of reference emailed to rxfellowships@butler.edu by October 30th, 2026
- Unofficial transcriptsSubmission of an unofficial application to Oracle will be used a placeholder. Please email your official transcript to rxfellowships@butler.edu by October 30th, 2026.
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Read the full posting here
Fellows will begin with the academic sector at Butler University for 4 months, move into their industry setting at Eli Lilly and Company for 12 months, and finish with an 8-month experience with the FDA.will continue to provide high-quality safety and regulatory experiences.