About The Position

The Clinical Research Coordinator handles or assists with the administrative activities generally associated with the conduct of clinical trials.

Requirements

  • High School Diploma or GED and three years of administrative support experience.
  • Or two years of college in a scientific, health related, or business administration program and one year of admin support or customer service experience.
  • Or be a licensed as a practical nurse (LPN) and one year admin support or one year of licensed practical nursing experience.
  • Or a Bachelor's degree, Master's degree, MD or PhD in a scientific, health related or business administration program.

Nice To Haves

  • Have Flow Cytometry experience.
  • Clinical specimen processing (fresh whole blood, PBMC, plasma, serum, urine, saliva, etc.).
  • Basic laboratory bench skills (micropipetting, aseptic technique, centrifugation, etc.).
  • BSL2 and/or BSL2-enhanced training.
  • Have experience with Microsoft applications.
  • Be able to have written and oral communication.
  • Be able to multitask.
  • Have organizational skills.

Responsibilities

  • Maintains data pertaining to research projects, completes source documents/case report forms, and performs data entry.
  • Assists with patient recruitment.
  • Attends study meetings.
  • Orders and maintains equipment and supplies.
  • Reviews medical records and/or conducts screenings for recruitment of study participants, performs interviews and QOL questionnaires.
  • Collects study specimen according to protocol which may include phlebotomy, processing, and preparation for shipping.
  • Coordinates services, schedules procedures, creates and maintains case packages, and monitors charges.
  • Assists with quality assurance and tracks regulatory submissions.
  • Performs related approved responsibilities as required.
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