About The Position

The Clinical Research Coordinator assists with the daily activities of clinical research studies, including obtaining informed consent, collecting and organizing study information, preparing tissue samples for analysis, and helping prepare grant applications and related documents for Institutional Review Board (IRB) and Grants and Contracts Office (GCO) processes. The role also supports participant screening and registration, clinical specimen handling, study documentation, and laboratory experiments.

Requirements

  • Bachelor’s or master’s degree in science or a closely related field.
  • No prior experience required.
  • Excellent written and oral communication skills.
  • Exceptional attention to detail.

Nice To Haves

  • One year of research experience preferred.
  • One to two years of previous clinical research experience.

Responsibilities

  • Collect and record study data and enter information into databases.
  • Obtain informed consent under minimal supervision of investigators and educate participants about study requirements.
  • Support clinical research activities, including answering phone calls, screening participants for eligibility, registering subjects with sponsoring agencies, and administering lifestyle questionnaires.
  • Assist with preparing grant applications and IRB/GCO submissions and filings.
  • Maintain source documents and subject files in accordance with hospital procedures, and ensure subject data are accurately and completely compiled through chart reviews.
  • Secure, deliver, and ship clinical specimens as required by study protocols.
  • Prepare for monitoring visits.
  • Perform other related duties, including preparing samples using standard immunological techniques and maintaining data and results from experiments.
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