The Institute for Genomic Medicine seeks to hire a skilled individual who
enjoys working with people and possesses 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.
Explain the research study to participants and facilitate digital
enrollment in the program if the participant is eligible.
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
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
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.
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 Clinical Research Coordinator will work independently as well as part
of a team.
Will be required to relate to diverse populations. S/he will connect with
participants to build report for long-term commitment to and engagement
with the All of Us Research Program. Communication skills include
excellent written communication skills, compassion, discretion, and
Perform other related duties as assigned.
Requires a bachelor's degree or equivalent in education and experience,
plus two (2) years of related experience. Related experience in clinical
The position requires excellent organizational, communication, and
interpersonal skills, attention to detail and the ability to work
Proficiency in Microsoft Office required.
Phlebotomy skills preferred; willingness to be trained as a phlebotomist
and ability to perform blood draws.
Bilingual in English/Spanish preferred, fluency in other languages will be
Equal Opportunity Employer / Disability / Veteran
Columbia University is committed to the hiring of qualified local residents.
Applications open: Sep 10 2021 Eastern Daylight Time
Senior Clinical Research Coordinator
The Senior Clinical Research Coordinator will work closely with the Principal
the Center for Prenatal Pediatrics (CPP).
clinical research in this space.
Explain all applicable study procedures, and consent eligible subjects...