Job Details

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.