Medicine
Position Summary
The Ethics Team at the Center for Precision Medicine and Genomics (CPMG) within Columbia University's Department of Medicine is seeking a dynamic and motivated Research Coordinator (Bioethics) to support and coordinate NIH-funded, community-engaged research studies.
This position involves a combination of independent and collaborative work under the supervision of Dr. Maya Sabatello, Principal Investigator. The Research Coordinator will support all aspects of the research portfolio, including literature reviews, qualitative and quantitative data collection, data analysis, manuscript preparation, professional presentations, and project administration.
The ideal candidate will have experience conducting empirical qualitative and quantitative research, familiarity with the ethical, legal, and social implications (ELSI) of genetics and genomics research, and a background in bioethics, public health, disability studies, or related social science disciplines.
For more information about CPMG, visit: https://columbiamedicine.org/cpmg/team.php.
Responsibilities
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 |
|---|---|---|---|
| Research Coordinator | Columbia University Medical Center | Psychiatry | The Department of Psychiatry is seeking a Research Coordinator to join our team in a full-time position to work within the division of Pathophysiology & Treatment Research. The Department of Psychiatry at the Vagelos College of Physicians & Surgeons of Columbia University is one of the largest in the country in terms of faculty size as well as state, federal, and foundation research support. Our mission areas include Healthcare, Education and Research. |
| 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. |
| IRB Specialist | Columbia University Medical Center | Institutional Review Board | The IRB Specialist of the Columbia University Human Research Protection Office (HRPO) reports to an IRB Senior Specialist-Manager. The IRB Specialist, working collaboratively with a team of other professionals, is primarily responsible for ensuring research protocols submitted for IRB review are assessed in an efficient manner for completeness, accuracy, and level of review according to applicable regulation and/or institutional policy; ensuring regulatory support is provided to a CU IRB with a large portfolio of research; coordinating convened, bi-weekly IRB meetings for review of research, as applicable; serving a resource for the CU research community, IRB Chairs and Members and the HRPO. |
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