At a Glance
- Tasks: Lead site monitoring for complex clinical trials and ensure compliance with regulations.
- Company: Join a dynamic global CRO with a focus on innovative research.
- Benefits: Competitive salary, travel opportunities, and professional growth.
- Other info: Collaborative team environment with opportunities to mentor junior CRAs.
- Why this job: Gain ownership of projects and make a real impact in rare disease studies.
- Qualifications: 3+ years of 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 Chester 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 East and Greater London area, this role not only provides meaningful work but also allows you to thrive in a community-focused environment.
