Position Summary
Research Assistant supporting clinical research studies through participant recruitment, screening, and coordination of study activities. Responsible for obtaining informed consent, conducting cognitive and neuropsychological assessments, and assisting with MRI/PET imaging procedures. Manages biological sample collection and processing, as well as data collection, entry, quality control, and secure storage. Ensures strict adherence to study protocols and data integrity standards, while contributing to regulatory submissions and ongoing study maintenance. Operates effectively in a fast-paced environment requiring strong organization, attention to detail, and the ability to manage multiple responsibilities.
Responsibilities
• Recruit, schedule, and communicate with study participants, ensuring informed consent and clear understanding of study procedures • Screen participants for eligibility through interviews and assist with in-person neuropsychological and cognitive assessments
• Administer computerized and paper-based tests, including tasks conducted during MRI sessions
• Collect, catalog, and process biological samples (e.g., blood) in accordance with study protocols
• Coordinate MRI and PET imaging appointments with external facilities
• Manage study data, including collection, entry, processing, storage, and quality control
• Maintain data integrity through accurate recordkeeping, database updates, and protocol compliance
• Support preparation and submission of study protocols, amendments, and renewals to IRB and regulatory bodies
• Run participant visits, complete assigned tasks, and provide regular updates to the research team and Principal Investigator
• Balance multiple responsibilities in a fast-paced environment while maintaining attention to detail and flexibility in scheduling
• Flexible work hours/possible weekend.
• Perform other related duties and responsibilities as assigned/requested.
Minimum Qualifications
Requires a bachelor’s degree and at least 1.5 years of related experience or equivalent in education, training and experience.
Preferred Qualifications
Phlebotomy certification is desirable but not required.
Flexible work hours
Equal Opportunity Employer / Disability / Veteran
Columbia University is committed to the hiring of qualified local residents.
| Title | Location | Department | Category | Employment Type |
|---|---|---|---|---|
| Research Coordinator | Columbia University Medical Center | Division of Scholarship & Rsch | Research (Lab and Non-Lab) | Full Time |
| Clinical Research Coordinator | Columbia University Medical Center | Pediatrics | Administrative Support, General Administration, Research (Lab and Non-Lab) | Full Time |
| Clinical Research Coordinator | Columbia University Medical Center | Pediatrics | Administrative Support, General Administration, Health/Clinical, Research (Lab and Non-Lab) | Full Time |
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