Regulatory Affairs Intern
Bristol Myers Squibb•Indianapolis, IN
•Onsite
About The Position
The Regulatory Affairs Intern will support the Regulatory Affairs team in preparing documentation, tracking submissions, and assisting with project coordination. This internship offers exposure to regulatory processes in the pharmaceutical industry and provides hands-on experience in a cross-functional environment. The full-time internship will take place June - August 2027 at our Indianapolis site.
Requirements
- Currently pursuing a Bachelor’s degree in Life Sciences, Pharmacy, Public Health, or related field
- Strong interest in regulatory affairs and drug development
- Excellent organizational and communication skills
- All candidates must be authorized to work in the US both at the time of hire and for the duration of their employment.
- Please note that immigration or visa sponsorship is not available for this position.
Nice To Haves
- Familiarity with Microsoft Office Suite (Word, Excel, PowerPoint, Outlook) and Adobe Acrobat
- Experience with project management tools (e.g., Smartsheet, MS Project) is a plus
- Prior internship or coursework related to clinical trials or regulatory science
- Detail-oriented and able to manage multiple tasks
- Strong written and verbal communication skills
- Professional, proactive, and eager to learn
- Ability to work collaboratively in a dynamic, cross-functional environment
Responsibilities
- Assist in organizing and formatting regulatory submission documents (e.g., IND, CTA, briefing packages, nonclinical reports)
- Help maintain submission trackers and document repositories
- Review documents for consistency and completeness under supervision
- Support the creation and updating of project timelines and task lists
- Attend team meetings and take notes on action items and follow-ups
- Help prepare meeting agendas and distribute materials
- Coordinate with internal teams to gather required documentation
- Draft internal communications and summaries for regulatory updates
- Shadow cross-functional meetings to understand regulatory integration
- Conduct literature reviews and regulatory intelligence gathering
- Assist in compiling summaries of relevant FDA/EMA guidance documents
- Help monitor changes in regulatory requirements and flag updates to the team
Benefits
- Limited benefits depending on program structure, work location, and local requirements.
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
Upload and Match Resume
What This Job Offers
Job Type
Full-time
Career Level
Intern
