About The Position

The Clinical Research Coordinator assists with the daily activities of clinical research studies, including obtaining informed consent and collecting, maintaining, and organizing study information. The role also prepares tissue samples for analyses and assists with grant applications and study-related documents for the Institutional Review Board and Grants and Contracts Office.

Requirements

  • Bachelor's or master's degree in science or a closely related field.
  • Excellent written and oral communication skills.
  • Exceptional attention to detail.

Nice To Haves

  • One year of research experience preferred.
  • Preferred 1–2 years of previous clinical research experience.

Responsibilities

  • Collect and record study data and enter information into databases.
  • Obtain informed consent under minimal supervision of the investigator(s) and educate participants about study requirements.
  • Support clinical research study activities, including answering phone calls, screening participants for eligibility, registering subjects with sponsoring agencies, and administering lifestyle questionnaires.
  • Assist in preparing grant applications and documents for Institutional Review Board and Grants and Contracts Office submission and filing.
  • Maintain source documents and subject files in accordance with hospital procedures.
  • Ensure accurate and complete compilation of subject data through chart reviews.
  • Secure, deliver, and ship clinical specimens as required by the protocol.
  • Prepare for monitoring visits.
  • Prepare samples using standard immunological techniques and maintain data and results from experiments.
  • Perform other related duties.
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