2027 Summer Intern Regulatory Affairs & Operations
Core
Support regulatory professionals in guiding medicine descriptions and approvals by health authorities, preparing and tracking submissions.
Role type
Summer Intern, Regulatory Affairs & Operations
Builds
Electronic regulatory documents, clinical trial application submissions, product labeling, and regulatory intelligence reports.
Domain
Pharmaceuticals / Life Sciences
Required skills
Research, writing, attention to detail, document formatting, cross-functional communication
Preferred skills
Interest in regulation or pharmaceuticals, demonstrated leadership
Technologies
Electronic regulatory document systems, clinical trial registration platforms
Responsibilities
Research global regulations, support clinical trial application submissions, format and publish electronic regulatory documents, gather regulatory intelligence, support product labeling, support clinical trial registration and results disclosure
Seniority
Intern