Clinical Research Associate, UK

Pharmaceutical Research Associates, Inc; Reading; Remote; GBP 40,000 - 60,000; Full time

Job summary

A leading biotechnology firm seeks an experienced Regional CRA to join their innovative team in the UK. This role involves monitoring clinical trials, supporting investigators, and ensuring compliance with study protocols. The position offers a rewarding opportunity to work with a global client and contribute to impactful research.

Qualifications

• Strong experience (>2 years) as a UK clinical research monitor.
• Current residence within the UK and appropriate right-to-work status.

Responsibilities

• Contributing to the selection of potential investigators.
• Providing monitoring visit reports within required timelines.
• Training and supporting investigators and site staff.

Skills

Monitoring

Data Verification

Job description

Overview

Experienced UK-based Regional CRA/clinical research associate required to augment 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 globally.

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

For this role, there is a requirement for only 1 internal interview with immediate feedback.

Responsibilities

Among other tasks, your main responsibilities will include:

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

Qualifications

Strong experience (>2 years) working as a UK clinical research monitor (or CRA), with current residence within the UK and appropriate right-to-work status.

Driving license required.

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