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Contract Research Organization

We understand your world - the pressures you’re facing on timelines, deadlines, and budgets - because we’ve done it ourselves. So we move fast and smart.

Deliver on Time & On Budget

With RBW, you’ll tap into a network of highly capable talent. But a successful hire isn’t just about knowledge & experience: we know you need people who can handle the pressures of regular bid defenses, tight schedules and budget constraints. Candidates who give you a potent value proposition. And one thing’s certain: they’re always in high demand.

That’s why we move proactively to grow our networks outside of specific assignments - so we know where to find the scarcest candidates and we’re never caught off guard. We can find you the right person for your culture, not just the right resume - and make sure it’s you they’re talking to first.

Why Choose Us

Our clients work with us time and time again because quite simply; we get them. Whether it’s being able to react quickly to an entire recruitment project, or finding that niche candidate for a role that doesn't exist yet, we are able to draw upon our vast candidate network to ensure we don't just find someone that can do the job, but also shares in the ideology of the company they are joining as well.

We represent agile organizations who support companies to deliver life changing innovation. We understand you need people who thrive in fast paced, ever-changing environments. Our team works extensively with innovators and providers supporting the life science industry, helping you meet your business goals.

You’ll get an agile, consultative hiring strategy that gives you the capability you need for today and the insight you need for tomorrow.

CRO Jobs

Principal Clinical Research Associate

£58-62,000 plus car allowance & bonus

RBW Consulting are excited to announce an opportunity on behalf of one of our close clients. This company are a renowned CRO with leading healthcare intelligence and a European culture. They treat unmet disease target areas and advance clinical research by providing outsourced services to pharmaceutical and biotechnology companies.

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; 6 years minimum
Broad knowledge of medical terminology and clinical patient management
Basic knowledge of drug therapy techniques and clinical research methodologies

To apply:

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

Apply Now Read More

Senior Clinical Research Associate

£50-56,000 plus car allowance & bonus

Job Title: Senior Clinical Research Associate
Location: Remote in England or South Wales
Salary: £50,000 - £56,000
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.

Join a highly experienced team dedicated to excellence in clinical research. 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; 4 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.

Apply Now Read More

Clinical Research Associate

£42-48,000 plus car allowance & bonus

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

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.

Apply Now Read More

Find More Jobs

CRO Jobs

Find More Jobs

Principal Clinical Research Associate

£58-62,000 plus car allowance & bonus

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; 6 years minimum
Broad knowledge of medical terminology and clinical patient management
Basic knowledge of drug therapy techniques and clinical research methodologies

To apply:

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

Apply Now Read More

Senior Clinical Research Associate

£50-56,000 plus car allowance & bonus

Job Title: Senior Clinical Research Associate
Location: Remote in England or South Wales
Salary: £50,000 - £56,000
Additional Benefits: Car allowance and bonus
Company: Global CRO

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; 4 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.

Apply Now Read More

Clinical Research Associate

£42-48,000 plus car allowance & bonus

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

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.