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Clinical research associate

Brighton
SoTalent
Clinical research associate
€50,000 a year
Posted: 12h ago
Offer description

Clinical Research Associate – Oncology (UK)


About the Role

An established global clinical research organisation is seeking a Clinical Research Associate (CRA) to join its Site Management (multi-sponsor) team, supporting Oncology clinical trials across the UK.

This role offers the opportunity to contribute to meaningful research that improves patient outcomes, while continuing to develop your monitoring expertise in a high-quality, regulated environment.


Key Responsibilities

* Conduct site monitoring visits (selection, initiation, routine monitoring, and close-out) in line with contracted scope and Good Clinical Practice (GCP)
* Support Oncology studies, ensuring protocol compliance and data integrity
* Partner with investigational sites to drive, adapt, and track patient recruitment plans
* Deliver protocol and study-specific training and maintain regular communication with sites
* Assess site quality and compliance with protocols, regulations, and ethical standards, escalating issues where required
* Track study progress including regulatory submissions, approvals, enrolment, CRF completion, and data query resolution
* Ensure accurate and compliant maintenance of the Trial Master File (TMF) and Investigator Site File (ISF)
* Prepare clear and timely monitoring visit reports, follow-up letters, and action plans
* Collaborate closely with cross-functional study team members to support delivery milestones


Requirements

* Proven experience independently monitoring Oncology clinical trials, including unblinded studies
* Strong working knowledge of ICH-GCP and applicable regulatory requirements
* Degree in Life Sciences or equivalent industry experience
* Flexibility and willingness to travel to sites across the UK
* Strong organisational, communication, and stakeholder-management skills

⚠️ Please note: this role is not eligible for visa sponsorship.


Why Apply

* Work on impactful Oncology studies
* Exposure to multi-sponsor trials and diverse site environments
* Strong focus on quality, learning, and professional development
* Opportunity to build a long-term career in clinical research
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