Clinical Research Associate

JR United Kingdom; Portsmouth; Remote; GBP 80,000 - 100,000; Full time

Job summary

Une entreprise croissante de recherche clinique recherche un Freelance Clinical Research Associate basé au Royaume-Uni. Ce poste, entièrement flexible, implique la surveillance de plusieurs sites d'essai clinique et offre une opportunité passionnante de travailler avec une équipe soudée tout en bénéficiant d'un salaire compétitif et de projets à long terme.

Benefits

Flexibilité de travail à distance

Salaire horaire compétitif

Possibilité de collaboration à long terme

Qualifications

• Au moins 2 ans d'expérience récente en tant que CRA au Royaume-Uni.
• Solide compréhension des GCP, des réglementations FDA et des processus d'essai clinique.
• Capacité à travailler de manière indépendante et à gérer plusieurs sites.

Responsibilities

• Surveiller les sites d'essai clinique aux différentes étapes du projet.
• Examiner les données sources et la documentation des sites.
• Identifier et suivre les problèmes ou écarts des sites.

Skills

Gestion des sites cliniques

Compréhension des réglementations GCP

Compétences en communication

Education

Baccalauréat dans les sciences de la vie ou le domaine connexe

Tools

Systèmes EDC

Job description

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Clinical Research Associate, portsmouth, hampshire

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Client:

Green Life Science

Location:

portsmouth, hampshire, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Views:

4

Posted:

31.05.2025

Expiry Date:

15.07.2025

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Job Description:

Now Hiring: Freelance Clinical Research Associate (CRA) – Remote (UK-Based)

Contract | Competitive Hourly Rate | Flexible Schedule

I'm working with a growing, full-service CRO that’s looking to bring an experienced Freelance CRA on board to support upcoming clinical trials. This is a great opportunity for someone who enjoys working independently, values flexibility, and wants to be part of a collaborative team environment.

About the CRO:

This is a small but expanding CRO that partners with biotech and pharma companies on early- to late-phase clinical trials. They’re known for being responsive, thorough, and committed to quality. As their study portfolio grows, they’re adding freelance CRAs to their network who can jump in and take ownership of site monitoring activities.

What You'll Be Doing:

• Monitor clinical trial sites across various stages—site selection, initiation, routine monitoring, and close-out
• Ensure sites are following protocol, GCP, and all applicable regulations
• Review source data, CRFs, and site documentation for accuracy and completeness
• Identify and follow up on any site issues or deviations
• Build strong working relationships with site staff
• Prepare and submit clear and timely visit reports
• Work closely with the internal clinical project team to keep things moving smoothly

What We're Looking For:

• At least 2 years of recent CRA experience in the U.k (independent or CRO-based)
• Strong understanding of GCP, FDA regulations, and clinical trial processes
• Background in life sciences, nursing, or a related field (Bachelor’s degree required)
• Able to work independently and manage multiple sites
• Comfortable with EDC systems and remote monitoring tools
• Based in the U.K. with ability to travel regionally as needed (up to ~60%)

Nice to Have:

• Experience with women's health, Neurology and Medical device
• Previous work with smaller CROs or sponsor teams
• A flexible, problem-solving approach

Why This Role?

• Competitive hourly pay
• Full remote flexibility + site travel
• Ongoing projects with potential for long-term collaboration
• A tight-knit team that values your input and expertise