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Clinical Research Coordinator

Company: Medix---
Location: Boca Raton
Posted on: November 23, 2022

Job Description:

We are looking for a full time onsite CRC to join a growing team at a CRO with a lot of room to grow. Previous experience in Clinical Research and direct patient care required. Great benefits and vacation package offered.
Essential Functions

  • Maintains detailed knowledge and understanding of assigned protocols, including all protocol requirements for patient/subject visits, obtaining informed consent, visit schedules, tests, procedures, laboratory information, and drug accountability requirements.
  • Responsible for creation of and ensuring the completion of all study documentation forms, including source documents and other study specific documents.
  • Coordinates and conducts patient/subjects' visit schedules and assures all procedures are conducted in compliance with the clinical protocol.
  • Collaborates with Principal Investigator as needed to assure that research participants receive appropriate medical evaluation and care when needed; alerts Principal Investigator of serious adverse events (SAEs).
  • Works with data management group to transcribe source data into eCRFs.
  • Works with sponsor Clinical Research Associate/study monitor to facilitate the sponsor monitoring and database clean-up process.
  • Attends sponsor Investigator/Study Coordinator meetings as needed for assigned protocols.
  • Conducts clinical research in compliance with all applicable regulations, including GCPs and company SOPs.
  • Demonstrates knowledge and application of all privacy and safety standards as they relate to job responsibilities, human research subjects, staff and the general operation of the unit.

Keywords: Medix---, Boca Raton , Clinical Research Coordinator, Healthcare , Boca Raton, Florida

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