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Clinical Research Coordinator job description

This Clinical Research Coordinator job description template can be used to advertise an open position in your company. Customize the requirements and responsibilities according to the needs of your specific role!
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Job brief

A clinical research coordinator with excellent organization and attention to detail is needed to join our research team.

You will manage and coordinate clinical research studies in your capacity as a clinical research coordinator.

You will work closely with research personnel, clinicians, and study participants to ensure that studies are executed safely, quickly, and in compliance with all regulatory standards.

Responsibilities

  • Develop and maintain study protocols and case report forms.
  • Recruit and screen study participants per study criteria.
  • Obtain informed consent from study participants and explain study procedures.
  • Collect and manage study data, including adverse events and other safety-related information.
  • Monitor study participant compliance and follow-up visits.
  • Manage study supplies, equipment, and inventory.
  • Assist with preparing and submitting study-related documentation to regulatory agencies and institutional review boards.
  • Collaborate with study sponsors and principal investigators to ensure that studies are conducted according to protocol.
  • Communicate study progress to research staff and other stakeholders.
  • Ensure that study data is collected and managed in accordance with regulatory requirements and study protocol.

Requirements

  • Bachelor's degree in a scientific or healthcare-related field
  • Minimum of 2 years of experience as a Clinical Research Coordinator or in a related role
  • Strong organizational and project management skills
  • Excellent attention to detail and accuracy
  • Strong communication and interpersonal skills
  • Ability to work well under pressure and within strict timelines
  • Familiarity with clinical research regulations, including FDA regulations and Good Clinical Practice (GCP) guidelines
  • Knowledge of clinical research protocols, case report forms, and study procedures
  • Proficiency in Microsoft Office and other relevant software applications

Note: Job requirements may vary depending on the employer and specific research setting. Certification in clinical research (e.g., Certified Clinical Research Coordinator or Certified Clinical Research Professional) is preferred.

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