Role OverviewThe Clinical Research Assistant supports the execution of clinical research studies by performing administrative, technical, and participant-focused tasks under the supervision of the Clinical Research Coordinator and Principal Investigator.
What You Will Do
Key responsibilities include study support and coordination, data and documentation, participant interaction, regulatory and compliance, and team collaboration.
Why It Might Be a Fit
The ideal candidate will have strong organizational, communication, and time management skills, with the ability to work accurately in a fast-paced environment with strong attention to detail.
Requirements
- Associate or bachelor’s degree in a health sciences, biology, psychology, or related field
- Previous experience in healthcare or research setting
- Familiarity with clinical trials, GCP, HIPAA, and human subjects research regulations
- Strong organizational, communication, and time management skills
- Ability to work accurately in a fast-paced environment with strong attention to detail
- Proficiency with Microsoft Office and data entry systems; experience with EDC or CTMS systems a plus
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