Clinical Research Associate, UK

ICON Strategic Solutions; United Kingdom; Remote; GBP 35,000 - 50,000; Full time

Job summary

A leading biotechnology company seeks an experienced Regional Clinical Research Associate (CRA) in the UK. This role involves monitoring clinical trials, supporting site staff, and ensuring compliance with study protocols. The position offers a strong internal support structure and the opportunity to work with a global client. Ideal candidates will have over two years of relevant experience and a valid UK driving license.

Qualifications

• Strong experience (>2 years) as a UK clinical research monitor.
• Driving License required.

Responsibilities

• Contribute to the selection of potential investigators.
• Provide monitoring visit reports within required timelines.
• Train and support Investigators and site staff.

Skills

Monitoring

Problem Solving

Communication

Job description

Experienced UK-based Regional CRA/clinical research associate required to augment existing CRA team, for multinational biopharmaceutical company partner.

You will be part of an innovative and global Biotechnology company, who pride themselves to be one of the world's leading independent biotechnology companies. They focus on areas with unmet medical need with the ambition to help reduce the social and economic burden of disease in society today.

This is a rewarding and interesting position with a key Global client, with a strong internal support structure in place (including a mentoring training plan) in a big team of ICON staff.

For this role - there is a requirement for 1x internal interview only (and immediate feedback).

Amongst other tasks, your main responsibilities will be to;

• Contribute to the selection of potential investigators.
• Provide the required monitoring visit reports within required timelines
• Drive performance at the sites. Proactively identify study-related issues and escalate as appropriate.
• Perform source data verification according to SDV plan and ensure data query resolution
• Initiate, monitor and close study sites in compliance with client Procedural Documents. Share information on patient recruitment and study site progress within local Study Delivery Team.
• Train, support and advise Investigators and site staff in study related matters.

Strong experience (~>2 years') working as a UK clinical research monitor (or CRA), and already residing within the UK (with appropriate right-to-work in the UK already granted, if applicable)

Driving License.

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