The role of clinical trial coordination

Clinical trial coordination supports the day-to-day conduct of a study. Coordinators work with investigators and research teams to organize participant visits, maintain study records, and keep activities aligned with the protocol. The work connects the participant experience with the practical requirements of research, keeping information, schedules, and follow-up actions organized.

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What the work involves

  • Coordinating participant visits, study procedures, and follow-up
  • Supporting recruitment and the informed consent process within delegated responsibilities
  • Maintaining study records and entering data into clinical trial systems
  • Tracking study requirements and communicating with investigators, monitors, and study teams
  • Documenting and escalating safety information and protocol deviations

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Roles within this pathway

Titles and responsibilities vary by employer.

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  • Clinical Research Coordinator (CRC): Coordinates study activities at a research site, working with participants, investigators, and study teams.
  • Assistant Clinical Research Coordinator: Supports participant scheduling, study documentation, data entry, and other delegated research activities.
  • Clinical Research Assistant: Provides practical and administrative support for research visits, records, and study procedures.
  • Research Nurse / Clinical Research Nurse: Combines nursing care with study coordination and protocol activities. These positions require the appropriate nursing qualifications and licensure.

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A pathway for diverse backgrounds

Clinical trial coordination draws on skills developed across healthcare, life sciences, public health, administration, and participant-facing work. Experience organizing information, communicating with people, and managing competing priorities provides a relevant foundation for supporting clinical studies.

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Accelerate your path into clinical trial coordination

Clintern Ascend combines industry training with a remote internship at a clinical research organization (CRO) partner. Apply your training through research workflows, study documentation, and study team support, without taking time off work or school. Dedicated résumé, interview, and career positioning support helps you communicate your experience to employers and pursue your next step with confidence.

Industry Perspectives

Hear why industry executives recommend Clintern Ascend and Clintern CRA Global, and explore their perspectives on clinical research and career preparation.
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Shelly Ikeme

Global Head, HEMA CSS

Johnson & Johnson

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Nina Clarke-Walker

Director of Clinical Operations

Syneos Health

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