Clinical Research Associate (CRA)
51231
Posted: 24/03/2026
- london, United Kingdom
- Contract
🔹 Clinical Research Associate (CRA)
📍 West London (Hammersmith area) | UK & Ireland travel
We are currently supporting a well-established, mid-sized Clinical Research Organisation in their search for a Clinical Research Associate (CRA) to join their growing team in West London.
This is an exciting opportunity to work within a collaborative environment on a diverse portfolio of clinical trials, including early and late-phase studies across a range of therapeutic areas, including rare diseases, medical devices, and non-interventional research.
The role offers flexibility, with hybrid or remote working options considered for the right candidate.
🔹 The Role
As a CRA, you will be responsible for overseeing clinical trial sites across the UK and Ireland, playing a hands-on role throughout the full study lifecycle—from feasibility and site selection through to study close-out.
You will work closely with Project Managers, sponsors, and site teams to ensure studies are delivered in line with regulatory requirements, timelines, and quality standards.
🔹 Key Responsibilities
🔹 About You
🔹 What’s on Offer
🔹 Apply
If you’re a motivated CRA looking to broaden your experience within a dynamic CRO environment, we’d love to hear from you. Please apply with your CV for a confidential discussion.
CBurton@barringtonjames.com
📍 West London (Hammersmith area) | UK & Ireland travel
We are currently supporting a well-established, mid-sized Clinical Research Organisation in their search for a Clinical Research Associate (CRA) to join their growing team in West London.
This is an exciting opportunity to work within a collaborative environment on a diverse portfolio of clinical trials, including early and late-phase studies across a range of therapeutic areas, including rare diseases, medical devices, and non-interventional research.
The role offers flexibility, with hybrid or remote working options considered for the right candidate.
As a CRA, you will be responsible for overseeing clinical trial sites across the UK and Ireland, playing a hands-on role throughout the full study lifecycle—from feasibility and site selection through to study close-out.
You will work closely with Project Managers, sponsors, and site teams to ensure studies are delivered in line with regulatory requirements, timelines, and quality standards.
- Support study start-up activities, including feasibility assessments and site identification
- Engage with potential investigator sites and contribute to site selection processes
- Coordinate and review essential regulatory documentation to support timely study activation
- Conduct site initiation, monitoring, and close-out visits in accordance with protocols and GCP guidelines
- Deliver site training and provide ongoing support to ensure protocol adherence
- Maintain and review Trial Master File (TMF) documentation to ensure audit readiness
- Oversee site performance, data quality, and patient safety throughout the study
- Build and maintain strong relationships with investigators and site staff
- Collaborate with internal teams and sponsors to ensure effective study delivery
- Bachelor’s degree in Life Sciences, Nursing, Pharmacy, Public Health, or a related discipline
- 1–2 years’ experience working as a Clinical Research Associate (or equivalent role)
- Hands-on experience with site monitoring, site initiation, and study documentation
- Solid understanding of ICH-GCP and clinical trial regulations
- Experience working with clinical systems such as EDC and CTMS
- Strong organisational skills with the ability to manage multiple priorities
- Excellent communication skills, both written and verbal
- Proactive, detail-oriented, and comfortable working both independently and as part of a team
- Additional European language skills are advantageous
- Must have the right to work in the UK
- Competitive salary and benefits package
- Private medical insurance, life assurance, and pension scheme
- Exposure to a wide range of clinical trials and therapeutic areas
- Supportive and collaborative team environment
- Opportunities for ongoing development and career progression
If you’re a motivated CRA looking to broaden your experience within a dynamic CRO environment, we’d love to hear from you. Please apply with your CV for a confidential discussion.
CBurton@barringtonjames.com
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