Regulatory Affairs Internship at Bristol Myers Squibb | Apply Now
A Bristol Myers internship opportunity has emerged for aspiring professionals as Bristol Myers Squibb seeks a Regulatory Affairs Intern for their Indianapolis location. This full-time internship will take place from June to August 2027, offering valuable experience in the pharmaceutical industry.
- Position: Regulatory Affairs Intern
- Location: Indianapolis – RayzeBio – IN
- Job Requisition ID: R1607433
About Bristol Myers Squibb
Bristol Myers Squibb is a global biopharmaceutical company dedicated to discovering, developing, and delivering innovative medicines that help patients prevail over serious diseases. With a purpose-driven culture, the organization emphasizes collaboration, accountability, and urgency in its work, providing employees with meaningful opportunities for growth and a supportive environment that values inclusion and well-being.
Bristol Myers Internship Description
The Regulatory Affairs Intern will support the Regulatory Affairs team in preparing documentation, tracking submissions, and assisting with project coordination. This Bristol Myers internship offers exposure to regulatory processes in the pharmaceutical industry and provides hands-on experience in a cross-functional environment.
Key Responsibilities
- Regulatory Documentation Support
- 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
- Project Coordination
- 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
- Cross-functional Communication
- Coordinate with internal teams to gather required documentation
- Draft internal communications and summaries for regulatory updates
- Shadow cross-functional meetings to understand regulatory integration
- Research and Compliance
- 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
Eligibility Criteria for Bristol Myers internship
- Currently pursuing a Bachelor’s degree in Life Sciences, 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.
Preferred Qualifications
- 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
Skills and Attributes
- 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
Bristol Myers Squibb hires for skills and capabilities, not just credentials – if this role excites you, but doesn’t perfectly match your resume, you are encouraged to apply anyway.
Compensation Overview: $24.00 – $45.00
This Bristol Myers internship is a significant step for those looking to advance their careers in regulatory affairs. Interested candidates are encouraged to apply before the deadline to seize this chance for professional growth in a leading biopharmaceutical company.
