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 |
|---|---|---|---|
| Clinical Research Coordinator I | Columbia University Medical Center | N/A | |
| Research Assistant | Columbia University Medical Center | NA | |
| Clinical Research Coord I | Columbia University Medical Center | Columbia University Irving Medical Center (CUIMC) provides global leadership in scientific research, health and medical education, and patient care. Working in the Department of Medicine under the direction of the Principal Investigator, the CRC will support coordination of clinical research activities for clinical research studies or trials managed by the Center of Quality Life and Aging. In general, the CRC 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. |
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