Clinical Research Associate, UK

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

You will be part of an innovative and global biotechnology company, 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.

This is a rewarding position with a key global client, supported by a strong internal team, including a mentoring and training plan.

The role requires only one internal interview with immediate feedback.

Main responsibilities include:

1. Contributing to the selection of potential investigators.
2. Providing monitoring visit reports within required timelines.
3. Driving site performance, proactively identifying issues, and escalating as needed.
4. Performing source data verification (SDV) and resolving data queries.
5. Initiating, monitoring, and closing study sites in compliance with procedural documents.
6. Training, supporting, and advising investigators and site staff on study matters.

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

Impactful work. Meaningful careers. Quality rewards.

At ICON, we value our employees and are committed to supporting your personal and professional growth. Whether leading a global team, becoming a scientific or technical expert, working in-house, or exploring different functions, we support your full potential.

Learn more about our culture at ICON and hear from CRA Debora Oh in Brazil about her tips for becoming a great CRA and her experience at ICON.