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Clinical research coordinator

Green Life Science
Clinical research coordinator
£45,000 - £55,000 a year
Posted: 3 October
Offer description

Clinical Research Coordinator – North of England

Location:
North West / North East England- Site-Based

Sector:
Clinical Research / Healthcare / Life Sciences

Employment Type:
Full-time, Permanent

About the Role:

We are currently partnering with a leading clinical research organisation (CRO) seeking a
Clinical Research Coordinator (CRC)
to join their expanding team in the
North of England
. This is an exciting opportunity to work at the forefront of clinical trials, supporting the delivery of high-quality research across therapeutic areas including oncology, neurology, and vaccines.

You'll play a pivotal role in coordinating the day-to-day operations of clinical studies at the site level—supporting both patients and investigators to ensure studies are conducted in line with Good Clinical Practice (GCP) and regulatory requirements.

Key Responsibilities:

* Coordinate and manage the daily operations of assigned clinical trials at the site
* Conduct patient screening, recruitment, informed consent, and scheduling
* Collect, record, and manage clinical data and source documents
* Liaise with Principal Investigators (PIs), Sub-Investigators, and sponsor representatives
* Maintain essential trial documentation (ISF, CRFs, logs) in compliance with GCP
* Report adverse events (AEs/SAEs) and ensure safety follow-up procedures are followed
* Assist with ethics and regulatory submissions as required
* Work closely with cross-functional teams including monitors, nurses, and project managers

Requirements:

* Previous experience working in a clinical research setting (site, NHS trust, CRO, or academic)
* Understanding of GCP and clinical trial protocols
* Strong patient-facing communication skills
* Detail-oriented with excellent organisational skills
* Proficient with clinical data systems (e.g. EDC, eSource)
* Life science, nursing, or healthcare degree preferred (or equivalent experience)

Desirable (Not Essential):

* ICH-GCP certification
* Phlebotomy or sample processing experience
* Experience in oncology, cardiovascular, or neurology trials
* NHS research site or SMO experience

What's in It for You:

* Competitive base salary + annual bonus
* 25–30 days annual leave + bank holidays
* Private healthcare + pension scheme
* Professional development & training support
* Opportunity to grow within a respected clinical research organisation
* Work on cutting-edge trials that make a difference in patients' lives

INTERESTED? APPLY NOW

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