Clinical Research Coordinator
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Requisition no: 525282
Work type: Full Time
Location: Medical Center
School/Department: Institute for Genomic Medicine
Grade: Grade 103
Categories: Research (Lab and Non-Lab)
Job Type: Officer of Administration
End Date if Temporary:
Hours Per Week: 35
The Institute for Genomic Medicine seeks to hire a skilled individual who
enjoys working with people and possess excellent interpersonal and
communication skills to work as a Clinical Research Coordinator for multi-year
research programs. The overall objective of this study is to obtain informed
consent to participate in research studies, including the All of Us Research
Program. The Clinical Research Coordinator will gather physical measurements,
blood pressure, collect biospecimens ( i.e., blood, saliva), and
administer study questionnaires to be used for future research purposes. New
patients will be approached in the outpatient clinics and inpatient setting.
The Clinical Research Coordinator will explain the research study to
participants and facilitate digital enrollment in the program if the
participant is eligible.
The coordinator will review and follow research protocols and determination
data management requirement for each patient enrolled; interacts with the
regulatory office to maintain regulatory documents and administrative files
for each protocol. Research coordination includes working with a research
nurse, treating physicians, and clinical team to facilitate confirm that each
patient meets eligibility criteria specified for protocols and enrollment into
the study. Both patient and regulatory research records will be maintained.
This involves working in conjunction with the study team to gather all
required data and relevant clinical information.
The incumbent will support the day-to-day recruitment of subjects for this
study, which include but are not limited to: active interaction with potential
participants in high-volume patient waiting rooms and via telephone,
participating in weekly meetings with enrollment team, data collection,
maintaining screening and recruitment logs, obtaining in-person informed
consent, collecting biospecimens ( i.e., blood, saliva, urine), assessing
and reporting barriers to recruitment.
The incumbent will perform other related duties as assigned.
The Clinical Research Coordinator will work independently as well as part of a
team. Coordinator will be required to related to diverse populations.
The Coordinator will connect with participants to build report for long-term
commitment to and engagement with the All of Us Research Program.
Communications skills include excellent written communication skills,
compassion, discretion, and follow-through.
Requires a bachelor's degree or equivalent in education and experience, plus
two years of related experience.
Related experience in clinical research preferred.
Phlebotomy skills preferred.
Bilingual in English/Spanish preferred, fluency in other languages will be
The position requires excellent organizational, communication, and
interpersonal skills, attention to detail and the ability to work
Proficiency in Microsoft Office required.
Willingness to be trained as a phlebotomist and ability to perform blood
Equal Opportunity Employer / Disability / Veteran
Columbia University is committed to the hiring of qualified local residents.
Applications open: Apr 29 2022 Eastern Daylight Time
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