How to match your resume to a Clinical Research Coordinator job description

We are looking for a Clinical Research Coordinator to recruit, consent and schedule trial participants. You will collect and enter study data accurately, and support investigators with regulatory and ethics submissions. Required: hands-on experience with Patient recruitment, Informed consent, Visit scheduling, Case report forms, and working knowledge of EDC systems, CTMS, Excel. Preferred: GCP Certification or BSc Life Sciences. Success in this role is measured by enrolment against target, data query rate, protocol deviations.

Required skills to mirror

• Patient recruitment
• Informed consent
• Visit scheduling
• Case report forms
• Sample handling
• GCP compliance
• Regulatory submissions
• Investigator support

Seniority ladder

• Research Assistant
• Clinical Research Coordinator
• Senior CRC

Title variants

• CRC
• Study Coordinator

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