At a Glance
- Tasks: Lead site monitoring for complex clinical trials and ensure compliance with regulations.
- Company: Join a growing global CRO with a collaborative and high-performing team.
- Benefits: Competitive salary, travel opportunities, and the chance to mentor junior CRAs.
- Other info: Dynamic role with opportunities for professional growth and exposure to complex studies.
- Why this job: Gain ownership of projects and make a real impact in rare disease studies.
- Qualifications: 3+ years of independent monitoring experience and strong knowledge of ICH-GCP.
The predicted salary is between 40000 - 50000 £ per year.
We’re supporting a growing, mid-sized, global CRO looking to hire a CRA II to support Phase I–IV and RWE studies. This is a hands-on role with full ownership of sites, working across complex and rare disease trials within a collaborative, high-performing team.
What you’ll be doing:
- Acting as the primary contact for assigned sites
- Delivering all monitoring visits (SIV, IMV, COV) to a high standard
- Supporting start-up, site selection and patient recruitment strategies
- Ensuring compliance with ICH-GCP, SOPs and regulatory requirements
- Managing TMF/ISF, IP accountability and site performance
- Identifying risks and driving solutions at site level
- Contributing to study delivery, data quality and timelines
- Mentoring junior CRAs and potentially leading projects
What we’re looking for:
- 3+ years’ independent monitoring experience
- Strong CRO background
- Experience in rare disease and/or transplant studies (pulmonary a bonus)
- Solid knowledge of ICH-GCP and regulatory frameworks
- Confident managing complex protocols and multiple sites
- South / South East / Greater London based
- Able to travel ~6–8 days/month
If you’re looking for more ownership, exposure to complex studies, and a role where you can genuinely add value — this could be a great next step.
Please apply here and Harry Henson will be in touch to discuss next steps.
CRA II - UK in Slough employer: RBW Consulting
Join a dynamic and supportive mid-sized global CRO that values collaboration and high performance, offering you the chance to take full ownership of your sites while working on complex and rare disease trials. With a strong emphasis on employee growth, you will have opportunities to mentor junior CRAs and lead projects, all within a culture that prioritises compliance and excellence in study delivery. Located in the vibrant South / South East / Greater London area, this role not only provides meaningful work but also allows you to thrive in a community-focused environment.
