Clinical Research Associate: Site Monitoring & Impact

Clinical Research Associate: Site Monitoring & Impact

Full-Time On-site
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TFS HealthScience is seeking a Clinical Research Associate to support delivery of clinical trials across designated sites in the United Kingdom. You will ensure patient safety, data quality, and protocol compliance while taking ownership of site management and relationships with investigators and site staff.

You will monitor trials according to ICH-GCP, build strong site partnerships, and proactively resolve site issues. Oncology and Phase I experience are a plus.

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Clinical Research Associate: Site Monitoring & Impact employer: TFS HealthScience

TFS HealthScience is an exceptional employer, offering a dynamic and supportive work environment that prioritises collaboration and innovation. With a strong commitment to employee growth, we provide comprehensive benefits and opportunities for professional development, ensuring that our team members can thrive in their careers while making a meaningful impact in the clinical research field. Join us in our mission to improve patient lives, where your contributions are valued and recognised within a culture built on trust and excellence.

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Contact Details:

TFS HealthScience Recruitment Team