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COORD CLINICAL RESEARCH II Location: Tampa, FL, US

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2019-12-24 08:01:42
Job Type: Full Time only

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The Clinical Trials Office Cutaneous Data Management program is looking for a Clinical Trials Coordinator.

Position Highlights

  • Maintain sound conduct of the clinical trial, including but not limited to recruitment, screening, education, enrollment, treatment and follow-up of eligible subjects according to protocol requirements.
  • Initiate study treatment related patient education per protocol.
  • Ensure timely source documentation of protocol standards is provided to facilitate data collection.
  • Coordinate and facilitate the execution of clinical trials within the designated program patient population.

Responsibilities

  • Coordinate clinical research protocols throughout all stages of the protocol.
  • Able to coordinate research patient care through the client system (to include ancillary departments).
  • Determines methods and procedures on new assignments.
  • Will interact directly with patients, managers and other department personnel.
  • Credentials And Qualifications
    Associates degree with 4-5 years of relevant clinical research experience required
    Bachelor\'s degree strongly preferred with at least 2 years relevant clinical research experience.
    CCRP/CCRC or equivalent preferred.

Key Skills: