2026 Summer Intern (Clinical Data Associate)
About The Position
We are currently seeking a highly motivated and talented intern to join data management team. This intern will learn about the development of EDC system, the study documents per protocol requirement. In addition, the associate will also learn to conduct the data review following the instructions from the study lead data manager on the study assigned. Our interns will assist with the daily operations in each of their specific departments assigned to and gain exposure, including but not limited to: Hands-on, meaningful work experience in their field of study. Work in the industry on applying leading edge technology. Use school knowledge in real-work situations. Explore the environment and culture of a leading biotechnology company. Develop a network of industry contacts for future mentorship and guidance. Provide qualified and enthusiastic candidates for short-term projects. Encourage word-of-mouth advertising when Interns return to school. Potential to bring new science technologies and knowledge from the classroom into the workplace. Each Intern is expected to prepare a short presentation to share what they have learned through their internship and how they hope their new knowledge will help them secure their future career. Presentations may be approximately 10-15 minutes long and should include visual aid (posters or PowerPoint).
Requirements
- Active undergraduate student with interests in clinical data management.
- Current enrollment in an undergraduate or graduate program with plans to return to school in the fall.
- Strong organizational and time-management skills.
- Excellent verbal and written communication skills.
- Ability to handle confidential information with discretion.
- All applicants must be at least 18 years of age by June 1, 2026.
- Provide adequate work authorization to work for any US employer through the duration of the program.
Nice To Haves
- Proficiency in Microsoft Office (Excel, Word, PowerPoint) is a plus.
Responsibilities
- Review the CRF and database specification to make sure the design matches the protocol requirements
- Help generate and review the edit check specification
- Support the sponsor UAT to make sure the validation on the key data points are complete and accurate
- Contribute to the study documentation and metrics
- Assist in the data management oversight data cleaning activities per the instruction from the study lead data manager on the study assigned.
Benefits
- Students will be on their own for housing, benefits, transportation, etc.
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What This Job Offers
Career Level
Intern
Education Level
Associate degree
Number of Employees
11-50 employees
