Clinical Research Associate (I, II, Senior) - UK

JR United Kingdom; England; On-site; GBP 30,000 - 50,000; Full time

Job summary

A leading biotechnology company is seeking a Clinical Research Associate (I, II, Senior) based in the UK. This role involves monitoring clinical trials, training site staff, and ensuring compliance with study protocols. Ideal candidates will have over 2 years of experience in clinical research monitoring and must reside in the UK.

Qualifications

• Strong experience (>2 years) as a UK clinical research monitor (CRA).
• Resident within the UK with appropriate right-to-work documentation.

Responsibilities

• Contributing to the selection of potential investigators.
• Providing monitoring visit reports within required timelines.
• Driving performance at the sites and proactively identifying study-related issues.

Skills

Monitoring visits

Data verification

Training

Problem-solving

Job description

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Clinical Research Associate (I, II, Senior) - UK, England

Client:

ICON Strategic Solutions

Location:

England, United Kingdom

Job Category:

Other

EU work permit required:

Yes

Job Views:

1

Posted:

25.05.2025

Expiry Date:

09.07.2025

Job Description:

Experienced UK-based Regional CRA/Clinical Research Associate required to augment an existing CRA team for a multinational biopharmaceutical company partner.

You will be part of an innovative and global biotechnology company, which prides itself on being one of the world's leading independent biotechnology firms. They focus on areas with unmet medical needs, aiming to reduce the social and economic burden of disease today.

This is a rewarding and interesting position with a key global client, supported by a strong internal structure, including a mentoring and training plan, within a large team of ICON staff.

For this role, there is a requirement for only one internal interview with immediate feedback.

Responsibilities include:

• Contributing to the selection of potential investigators.
• Providing monitoring visit reports within required timelines.
• Driving performance at the sites and proactively identifying study-related issues for escalation.
• Performing source data verification according to SDV plan and resolving data queries.
• Initiating, monitoring, and closing study sites in compliance with client procedures. Sharing information on patient recruitment and site progress within the local Study Delivery Team.
• Training, supporting, and advising investigators and site staff on study-related matters.

Requirements:

• Strong experience (>2 years) as a UK clinical research monitor (CRA).
• Resident within the UK with appropriate right-to-work documentation.