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Northwestern University

Research Study Coordinator

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What they do

A Clinical Research Coordinator directs clinical research and development projects for companies, and coordinates testing and quality control.

$109,886 / year median in Illinois

+8% projected growth

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Job Description

at Northwestern University in
Evanston, Illinois, United States Job Description Job Opening Id:
54209
Department:
MED-Preventive Medicine Salary/Grade:
NEX/11 arget hiring range for this position will be between $41,371 - $59,311 per year. Offered salary will be determined by the applicant's education, experience, knowledge, skills and abilities, as well as internal equity and alignment with market data.
Job Summary:
Performs biomedical &/or social-behavioral research by administering tests &/or questionnaires following protocols; collecting, compiling, tabulating &/or processing responses; gathering information; &/or assisting in the preparation of material for inclusion in reports. Completes all activities by strictly following Good Clinical Practices (GCP) & all relevant current local, state, & federal laws, regulations, guidance, policy & procedure developed by the NU Institutional Review Board (IRB), Food & Drug Administration (FDA) Code of Federal Regulations (CFR), & the International Conference on Harmonization (ICH). The Research Study Coordinator performs recruitment and data collection for the
MESA MIND
Research Study at Northwestern University under the direction of the Project Manager and PI. The Research Study Coordinator is a part of a team responsible for scheduling appointments, collecting samples, and recording data. The Research Study Coordinator position also requires traveling to participant homes throughout Chicagoland and suburbs to conduct study visits.
Specific Responsibilities:
Technical Reviews & obtain informed consent. Schedules study visits with participants. Conduct interviews. Scores test results. Collects survey data. Facilitates communication with key personnel & participants to maintain project study flow. Enter all data into multiple databases, spreadsheets, and calendars. Performs blood draws, urine collection and processing, and all aspects of research participants' visits, including height, weight, blood pressure, questionnaire administration, and cognitive function testing. Participate in study meetings Administration Prepare the charts for the participant visits, set up and clean exam rooms before and after visits, enter data as needed, perform data and equipment quality control checks, etc.&nbs To view full details and how to apply, please login or create a Job Seeker account