Taub Inst Res Alzheimers Disease Aging Brain
Position Summary
The Research Assistant will support innovative Huntington’s disease clinical trials and observational studies by assisting with participant recruitment, data collection, neuropsychological assessments, and biospecimen processing. This is an exciting opportunity to contribute to research aimed at advancing the understanding and treatment of Huntington’s disease while working within a collaborative, multidisciplinary research team.
Responsibilities
Responsibilities involving recruitment, questionnaires, neuropsychological testing, data entry and biofluid handling. The research assistant will work under the supervision of the Senior Research Managers and the study Principal Investigator.
The position involves roles and responsibilities that include, but are not limited to:
• Screen charts, recruit, schedule, and consent subjects for studies.
• Prepare for upcoming study visits.
• Conduct clinical interviews with study participants and use study-specific assessments, review of medical history, cognitive and neuropsychological testing, and other questionnaires.
• Process blood and other biological samples such as cerebrospinal fluid (CSF) and urine as per study procedures.
• Perform ECGs on study participants
• Accurately collect and enter data into databases and electronic case report forms.
• Adherence to federal and institutional regulations and GCP guidelines.
• Assist with other administrative and research activities as required.
• Assist in the maintenance, programming, and management equipment used to collect data such as laptops, tablets, and devices distributed to participants for passive monitoring of movements and activities such as smartphones and smartwatches provided by the study.
• Perform other related duties and responsibilities as assigned/requested.
Minimum Qualifications
Preferred Qualifications
Other Requirements
Equal Opportunity Employer / Disability / Veteran
Columbia University is committed to the hiring of qualified local residents.
| Title | Location | Department | Summary |
|---|---|---|---|
| Clinical Research Coordinator I | Columbia University Medical Center | Herbert Irving Comprehensive Cancer Center | In general, the CRC I will be responsible for the coordination of patient participation (including screening, recruitment, assessment, and follow-up of study participants), collection and maintenance of study data, ensuring adherence to study activities as described in the protocol, and working with other members of the research team to coordinate all other aspects related to the conduct of the clinical trial or study. This position is primarily based out of the Herbert Irving Pavilion, 161 Fort Washington Avenue, Mezzanine level, New York, NY. Subject to business needs, we may support flexible and hybrid work arrangements. Options will be discussed during the interview process. |
| Clinical Research Coord I | Columbia University Medical Center | Pharmacology | The Clinical Research Coordinator I will serve as the clinical coordinator for the Abate-Shen and Shen Labs and the central liaison for the Mark Foundation Center for Lineage Plasticity at Columbia University Irving Medical Center (CUIMC), supporting translational and clinical research studies in urologic and genitourinary oncology. This role will manage day-to-day study operations across multiple protocols, including patient-facing coordination, biospecimen collection, and clinical data management. This role will work closely with physicians, surgeons, research staff, and external partners to ensure high quality data collection and regulatory compliance. This role will coordinate complex workflows across concurrent studies, applying judgment to prioritize tasks and address challenges as they arise; it will also contribute to process improvements and support guidance of new research staff. |
| Non-Student Short-Term Casual | Columbia University Medical Center | Gertrude H. Sergievsky Center | NA |
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