Clinical Research Coordinator

Green Life Science; United Kingdom; Hybrid; GBP 60,000 - 80,000; Full time

Job summary

A growing clinical research organization in the UK is seeking a Clinical Research Coordinator to deliver high-quality, GCP-compliant clinical trials across multiple therapeutic areas. The role involves supporting investigators, ensuring patient safety, and managing various trial activities. Candidates should possess a degree in Life Sciences or a related field and have prior experience in clinical research. Excellent organizational and communication skills are essential. Competitive salary and career progression opportunities are offered.

Benefits

Competitive salary

Annual performance-based bonus

Career progression opportunities

Supportive and collaborative environment

Qualifications

• Prior experience in clinical research as CRC, CTA, CRA, or Research Nurse is essential.
• Strong knowledge of UK regulatory frameworks is necessary.

Responsibilities

• Coordinate day-to-day delivery of clinical trials in line with study protocols.
• Assist with study start-up and site initiation.
• Manage investigational product handling and data integrity.

Skills

Organisational skills

Communication skills

Interpersonal skills

Knowledge of ICH-GCP

Adaptability

Education

Degree in Life Sciences, Nursing, or equivalent

Job description

Location: Multiple sites across the UK (Relocation may be required)

Salary: Competitive base + annual bonus + full benefits

Contract: Permanent, full-time

Interview Process: Fast-track interviews available – apply now!

About the Role

We’re proud to be recruiting on behalf of a growing clinical research organisation with an expanding network of investigator sites across the UK.

This is an exciting opportunity for a Clinical Research Coordinator (CRC) to play a key role in the delivery of high‑quality, GCP‑compliant clinical trials across multiple therapeutic areas.

You’ll be at the heart of clinical trial activity — supporting investigators, ensuring patient safety, and helping bring new treatments to patients faster.

Key Responsibilities

• Coordinate the day‑to‑day delivery of clinical trials in line with study protocols, ICH‑GCP, and MHRA/HRA regulations.
• Assist with study start‑up, feasibility, ethics submissions, and site initiation.
• Support investigators with patient recruitment, consent, scheduling, and follow‑up visits.
• Maintain accurate and timely source documentation, CRFs, and site files.
• Manage investigational product handling, sample collection, and data integrity.
• Act as a key liaison between sponsors, CROs, monitors, and internal teams.
• Support quality assurance, audits, and inspections as required.
• Contribute to continuous process improvement and patient engagement initiatives.

About You

• Degree in Life Sciences, Nursing, or equivalent healthcare qualification.
• Prior experience working in clinical research (as CRC, CTA, CRA, or Research Nurse).
• Strong knowledge of ICH‑GCP and UK regulatory frameworks.
• Excellent organisational, communication, and interpersonal skills.
• Proactive, adaptable, and able to manage multiple priorities.

What’s on Offer

✅ Competitive salary aligned with experience and regional benchmarks.

✅ Annual performance‑based bonus.

✅ Clear career progression and professional development opportunities.

✅ Exposure to a wide variety of therapeutic areas and study phases.

✅ Supportive and collaborative environment focused on quality and innovation.