Clinical Research Coordinator CV example, template, and formatting tips to help you present your UK research experience clearly and professionally. This guide provides practical examples of professional summaries, work experience bullets, and section order so you can tailor your CV to NHS hiring managers and study teams.
You'll find concrete phrasing for common CRC responsibilities and clear formatting that keeps your CV scannable for busy recruiters.
Building a Clinical Research Coordinator resume?
Skip the blank page. Start with a template built for this role, then tailor it for each job you apply to.
Clinical Research Coordinator CV Template
Preview the template, then edit it in JobCopy for your experience.
Tip: use the template as a starting point, then swap in your own numbers and project names.
Clinical Research Coordinator CV example: Template and section order
Use a clear, conventional layout so hiring managers find what they need quickly. Start with a contact line including your name, address in the UK, telephone, and email, then a concise professional summary, followed by Key Skills, Clinical Research Experience, Education, Certifications and Trainings, and any Additional Relevant Experience or Volunteering.
Keep each section labelled and consistent so your CV scans well for both humans and applicant tracking systems (ATS).
Below is a simple section order you can follow for a Clinical Research Coordinator CV. Use headings that match the job posting terminology to help your application align with the role.
Examples
Contact
Professional Summary
Key Skills
Clinical Research Experience
Education
Certifications and Training
Additional Relevant Experience or Volunteer Work
Clinical Research Coordinator CV example: Professional Summary and profile statements
Your professional summary should be 2-3 concise sentences that highlight your experience co‑ordinating study operations in UK settings and ensuring protocol compliance within the regulatory framework. Refer to the NHS, HRA, REC, and MHRA where relevant and mention patient safety and data integrity.
Use a confident, practical tone so a hiring manager can picture you contributing from day one.
Example summary phrasing might describe your co-ordination of regulatory documents, IRAS submissions, and collaboration with investigators and trial sites to support recruitment and retention targets.
Examples
Organised Clinical Research Co‑ordinator with experience supporting Phase II and III oncology and cardiology trials, managing source documentation and site visits.
Detail‑oriented co-ordinator who maintains regulatory binders, prepares IRAS submissions, and collaborates with cross‑functional teams to meet recruitment goals.
Work experience examples for Clinical Research Coordinator CV
Write each role with a brief context line and 3-5 achievement‑oriented bullets that begin with strong verbs and explain your impact. Use UK spellings and action words such as co‑ordinated, organised, managed, prepared, audited, monitored, and liaised with investigators, sites, and sponsors.
Include dates in DD/MM/YYYY format and reference UK regulatory activity where possible.
Examples
Clinical Research Co‑ordinator, NHS Trust, 01/06/2020 – 31/08/2024. Supported Phase II oncology trial sites, ensured regulatory compliance, and completed source data verification with 99% accuracy.
Co‑ordinated regulatory submissions and site visits across five study sites, maintained essential regulatory binders, and supported patient recruitment by 15%.
Liaised with Principal Investigators and sites to ensure timely protocol amendments and safety reporting to the trial sponsor.
Additional Tips
- 1Prioritise recent clinical research experience and list the most relevant roles first, especially for NHS or UK employer requirements.
- 2Limit jargon; spell out acronyms on first use to help HR and non‑specialist readers.
- 3Include a concise Key Skills section near the top to help both ATS filters and recruiters.