RBW Consulting logo

Clinical Research Associate

RBW Consulting
Department:Administrative
Type:REMOTE
Region:UK
Location:United Kingdom
Experience:Mid-Senior level
Salary:£42,000 - £48,000
Skills:
CLINICAL RESEARCHSITE MANAGEMENTMONITORING VISITSREGULATORY COMPLIANCESOURCE DOCUMENT VERIFICATIONADVERSE EVENT REPORTINGPATIENT RECRUITMENTCAR-T THERAPIESPHASE 1-3 TRIALS
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Job Description

Posted on: March 21, 2026

  • Job Title: Clinical Research Associate
  • Location: Remote in England or South Wales
  • Salary: £42,000 - £48,000
  • Additional Benefits: Car allowance and bonus
  • Company: Global CRO

RBW Consulting is thrilled to present an exciting opportunity on behalf of one of our esteemed clients. As one of the few rapidly growing Contract Research Organizations (CROs) for UK studies, our client is expanding their site management team with multiple hires this year. They are involved in a diverse range of studies, including cutting-edge research in advanced therapies such as CAR-T.

In this role, you will benefit from a supportive management team committed to your professional growth. They provide clear guidance on the skills needed for advancement and offer fluid career development opportunities across various departments.

This company prioritizes quality over metrics and is currently generating significant excitement within their UK team.

Key accountabilities

  • Autonomy of investigator sites with full responsibility for the successful management of sites through study life cycle (start-up to close-out);
  • Conduct feasibility, pre-study, initiation, monitoring, and closeout visits for research sites, mainly phase 1 to 3 and within all available therapeutic areas;
  • Prepare accordingly and attend investigator meetings, coordinating timely delivery and subsequent proper storage and accountability of clinical supplies and following-up of drug safety issues;
  • Perform source document verification and case report form review;
  • Perform regulatory document review;
  • Conduct study drug inventory;
  • Perform adverse event and serious adverse event reporting and follow-up; and
  • Assess patient recruitment and retention.

Qualifications

  • Bachelor of Science in health-related field (or equivalent)
  • Proven CRA experience; 2 years minimum

Why Join?

  • Supportive Environment: Build strong relationships with a transparent management team focused on your development.
  • Innovative Approach: Work with a company that embraces a 360 monitoring approach and leverages AI to enhance efficiency and save time.
  • Results-Driven KPIs: Our client's key performance indicators are centered around tangible study outcomes, such as patient recruitment, visit reports, and resolving site issues.
  • Administrative Support: Dedicated admin staff to help with site management tasks, helping to maintain a balanced workload.
  • Training: Extensive training and buddy system in place.
  • Career Growth: promotion opportunities up to 4 times a year.
  • Therapy Areas: Access to mixed therapy areas, including advanced therapies like CAR-T.

To apply

Please click ‘apply’ or contact Harry Henson for any further information.

Originally posted on LinkedIn

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