Clinical Research Coordinator (CRC)

Alternate titles:

Clinical Trials Coordinator

General role description

Clinical Research Coordinators (CRCs) support the day-to-day running of clinical research studies. They help organise participant visits, carry out participant assessments, and manage study records. CRCs work closely with researchers, healthcare staff, and partner organisations to make sure research is carried out safely, ethically, and in line with the study plan.

Key responsibilities

  • Coordinate clinical trial activities, including recruitment and enrolment of participants
  • Maintain accurate study records and documentation in line with regulatory requirements
  • Support ethics submissions and assist with trial administration
  • Assist with participant visits, assessments, and the collection of participant samples (e.g. blood samples)
  • Liaise with internal and external partner teams to ensure the study runs smoothly
  • Ensure participant confidentiality and adherence to research protocols

Workplace settings

  • Universities and Medical Research Institutes
  • Pharmaceutical, Biotechnology and Medical Device Companies
  • Contract Research Organisations (CROs)
  • Not-for-profit, Government, Peak Body, Advocacy and Other Research-Performing Organisations
  • Healthcare Settings

Required qualifications

  • A degree in health sciences, biomedical sciences, nursing, or a related field is often preferred

Other notable requirements

CRCs often need:

  • Understanding of Good Clinical Practice (GCP) principles
  • Strong organisational and time management skills
  • Attention to detail and ability to follow research protocols
  • Effective communication and stakeholder coordination skills
  • Awareness of ethical conduct in human research

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