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Role Summary
Summer 2026 - Clinical Research and Development Internship
Responsibilities
Reviews literature and prepares summary documents for inclusion in Investigator Brochure, protocols, regulatory submission documents, etc.
Assists Clinical Scientist and/or Clinical Trial Physician in making recommendations and providing clinical research expertise related to projects.
Assists with preparation and review of key documents e.g., protocols, protocol amendments, IBs, regulatory submission documents, internal or external presentations, clinical study reports etc.
Assists with organization and review of ongoing summary data including safety, primary efficacy variables, laboratory data, and clinical narratives.
Qualifications
Current undergraduate student majoring in life science, biology, cell biology, and related fields.
All candidates must be authorized to work in the US both at the time of hire and for the duration of their employment. Immigration or visa sponsorship is not available for this position.