Clinical Study Coordinator

1 month ago


Detroit, Michigan, United States Proclinical Full time

Welcome to Proclinical, a leading recruitment agency in the pharmaceutical and medical industries. We are currently looking for a dedicated Clinical Study Coordinator to join our team. This role involves coordinating clinical research projects, providing technical support to Principal Investigators, and ensuring compliance with regulations. The successful candidate will also be responsible for quality assurance measures, reporting adverse events, and serving as a liaison between the institution and sponsor.

Responsibilities:

  • Coordinate clinical research projects in compliance with regulations.
  • Provide technical support to Principal Investigators.
  • Implement quality assurance measures.
  • Report adverse events to relevant authorities.
  • Coordinate external audits and monitoring visits.
  • Serve as a resource for the department and organization.

Requirements:

  • Bachelor's degree in a related field.
  • Strong organizational and problem-solving skills.
  • Excellent communication skills.
  • Previous coordinator experience is beneficial.
  • Certifications such as SOCRA, ACRP, and IATA are preferred.

If you are interested or have any questions, please contact our team. Proclinical Staffing is an equal opportunity employer.



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