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S

Clinical Research Associate

SoTalent Brighton


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    S

    Clinical Research Associate

    SoTalent Brighton
    Status Open
    Apply now

    Apply on the employer's website


    What we ask

    Education

    No minimum education required

    Job 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

    About the employer

    SoTalent
    Apply now

    Apply on the employer's website

    Apply now

    Apply on the employer's website


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