Regulatory Affairs Intern: Submissions & Coordination

Bristol Myers Squibb; Indianapolis (IN); Sur place; USD 33 000 - 62 000; Plein temps

Résumé du poste

Bristol Myers Squibb in Indianapolis is offering a full-time Regulatory Affairs Intern position for a June–August 2027 internship at our Indianapolis site. The role supports the Regulatory Affairs team with documentation, submissions tracking, and project coordination in a cross-functional environment.

Ideal candidates are pursuing a Life Sciences-related degree, eager about regulatory affairs, and possess strong organizational and communication skills. US work authorization is required.

Qualifications

• 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.
• Authorized to work in the US without visa sponsorship.

Responsabilités

• 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 and timeline management.
• Attend team meetings and take notes on action items and follow-ups.
• 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.
• Monitor changes in regulatory requirements and flag updates.

Connaissances

Organizational skills

Communication skills

Regulatory affairs interest

Formation

Bachelor’s degree in Life Sciences, Pharmacy, Public Health, or related field

Outils

Microsoft Office

Adobe Acrobat

Smartsheet

MS Project

Description du poste

Bristol Myers Squibb in Indianapolis is offering a full-time Regulatory Affairs Intern position for a June–August 2027 internship at our Indianapolis site. The role supports the Regulatory Affairs team with documentation, submissions tracking, and project coordination in a cross-functional environment.

Ideal candidates are pursuing a Life Sciences-related degree, eager about regulatory affairs, and possess strong organizational and communication skills. US work authorization is required.