Environmental Health Sciences
Position Summary
The Research Assistant will work in the Columbia Center for Children’s Environmental Health (CCCEH) in the Department of Environmental Health Sciences, at the Mailman School of Public Health. The RA will be expected to help run participant visits from the Fair Start and Sibling Cohorts as part of two federally funded research grants. The purpose of this study is to assess the effects of environmental exposures on women and their children in Northern Manhattan and South Bronx. The candidate will be responsible for a variety of administrative and research tasks, including consenting study participants, scheduling, arranging transportation, interviewing participants, administering psychological and psychodiagnostics assessments, administering psychological, behavioral, and environmental rating scales. In particular, candidate will be conducting diagnostic clinical interviews with mothers/caregivers. Candidate will also be responsible for processing, storing, checking data and transferring data to the Center’s data management core and/or laboratory.
The candidate will assist with human subjects research and administrative duties as needed to maintain a caseload of research participants enrolled in a longitudinal birth cohort.
Responsibilities
Minimum Qualifications
Preferred Qualifications
Equal Opportunity Employer / Disability / Veteran
Columbia University is committed to the hiring of qualified local residents.
| Title | Location | Department | Summary |
|---|---|---|---|
| Clinical Research Coord I | Columbia University Medical Center | Medicine | 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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