Clinical Study Coordinator

PSI CRO AG
Any Location, FL
Category Research
Job Description
The Site/Study Coordinator supports a medical institution in clinical trial-related activities, including protocol-specific tasks, data entry, and communication with sponsors and CRO representatives. The role involves mentoring staff, administrative tasks, and ensuring compliance with local and federal laws and regulations.

Requirements

  • Relevant education and at least two years of experience coordinating clinical research studies involving human subjects
  • Bilingual proficiency in English and Spanish
  • Current Good Clinical Practice (GCP) certification
  • International Air Transport Association (IATA) certification
  • Current Basic Cardiopulmonary Resuscitation (CPR) certification
  • Phlebotomy certification unless part of active professional licensure (RN or LPN)
  • Preferred Certification in Clinical Research by ACRP or SOCRA or another approved Clinical Research Organization

Benefits

  • Full-time position
  • On-site location in Coral Springs, Florida
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