Clinical Research Coordinator

1 day ago


tampa, United States X4 Life Sciences Full time

A growing Clinical Site is seeking a Clinical Research Coordinator (CRC) to join its dynamic team in Tampa. The CRC will be responsible for screening, enrolling, and providing follow-up care for study participants, ensuring strict adherence to study protocols and regulatory standards, while closely monitoring participants throughout the trial.


Primary Responsibilities:

  • Ensure compliance with FDA regulations and ICH guidelines in all clinical trial activities.
  • Obtain informed consent from study participants.
  • Perform visit procedures, including accurate collection, processing, and shipping of specimens according to protocol.
  • Carry out basic clinical tasks such as blood draws, monitoring vital signs, and administering ECGs.
  • Identify and report Adverse Events (AEs) and Serious Adverse Events (SAEs) to the Principal Investigator.
  • Schedule and organize patient visits within specified timeframes.
  • Dispense study medications in line with protocol and educate participants on correct usage and adherence.
  • Track and document participant progress on study medications.


Qualifications:

  • 1-4+ years of experience as a Clinical Research Coordinator.
  • Phlebotomy experience.
  • Good Clinical Practice (GCP) certification.
  • In-depth knowledge of federal regulations and GCP standards.
  • Strong interpersonal skills, attention to detail, and exceptional record-keeping abilities.
  • Bi-lingual proficiency (preferred).


Candidates with a passion for clinical research and the relevant qualifications are encouraged to apply. This is an opportunity to be part of a team committed to advancing medical research and making a meaningful difference.



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