Clinical Development Internship (Undergraduate)
Biodesix, Inc.
Louisville, COFresher2h agovia LinkedIn
This job at a glance
- Who can apply
- New grads and up to 1 year · Bachelor's degree
- Must know
- GCPOperationsExcelMicrosoft Office
- Nice to have
- Patient care
- Work
- On-site in Louisville · internship
- Pay
- Not stated by the employer.
- Skill demand
- Operations47%Microsoft Office28%Excel22%GCP21%of 99 similar entry-level jobs posted in the US this week
- Listed
- Nov 2, 2026 · still open
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About the Role
As a Clinical Development Intern, you will support projects focused on clinical site quality, regulatory documentation, and study performance. You will gain exposure to clinical research operations, Good Clinical Practice (GCP) standards, and the processes that ensure the quality and compliance of clinical studies.
Key Responsibilities
- Review regulatory and study documentation for completeness, accuracy, and filing consistency.
- Support Trial Master File (TMF) and Investigator Site File (ISF) quality review activities.
- Identify missing documentation and assist with document tracking efforts.
- Review site regulatory document inventories and verify expiration dates for licenses, CVs, GCP training records, and related documentation.
- Develop and maintain quality metrics, scorecards, and tracking tools.
- Analyze site performance trends, protocol deviations, and operational data.
- Create regulatory filing checklists and support continuous improvement initiatives.
- Present project findings and recommendations at the conclusion of the internship.
Requirements & Tech Stack
- Microsoft Excel (filtering, sorting, formulas, Pivot Tables)
- Microsoft Word
- Microsoft PowerPoint
Qualifications
- Currently pursuing a Bachelor of Science degree in Molecular Cell Biology, Biology, Integrative Physiology, Biochemistry, Biomedical Science, or a related field.
- Strong attention to detail and organizational skills.
- Ability to maintain confidentiality and handle sensitive information appropriately.
- Strong written and verbal communication skills.
- Ability to manage multiple priorities and work independently with guidance.
- Interest in clinical research, healthcare, regulatory affairs, or quality systems, preferred.
- Strong research and information-gathering skills, preferred.
Program Details
- Location: On-Site in Louisville, CO
- Program Dates: May 17 to August 6, 2027
- Time Commitment: 20 to 40 hours per week
- Compensation: $19.00 per hour
- Deadline to Apply: December 11, 2026