464 Clinical Research Associate jobs in the United Kingdom

Clinical Research Associate (CRA) – Hybrid – London Region

RBW Consulting is excited to announce an opportunity on behalf of a small CRO client we are partnered with. This company focuses on UK-based studies and site visits are regionally based around the London area.

This opportunity offers exposure to varied therapy areas, manageable site visits, and the chance to develop beyond traditional monitoring responsibilities.

The Role

You’ll be working on a broad portfolio of studies, from initiation through to close out, across multiple therapy areas including respiratory and emerging fields. This hybrid position involves monitoring sites (primarily in and around London) and attending the office approximately twice per month.

Key responsibilities include:

• Monitoring visits at UK trial sites
• Setting up, managing, and maintaining eTMFs
• Ensuring delivery of studies within budget and timelines
• Liaising with sponsors, vendors, and internal teams to maintain project oversight
• Supporting colleagues through training and mentoring in areas of expertise
• Contributing to project, client, and team meetings

What We’re Looking For

• At least 1 year experience as a CRA (can consider candidates with academic or industry experience)
• A proactive approach with the flexibility to handle multiple priorities in a dynamic environment

The Offer

• Salary range: £40,000–£47,000 , with potential annual increases
• 25 days annual leave plus standard benefits
• Hybrid working model (office attendance twice per month)
• Opportunities for professional growth, with development into Senior CRA or Project Management roles

This role is ideal for CRAs who enjoy a mix of independence and collaboration, and who want to be part of an organisation that values quality, career growth, and work-life balance.

To apply:

Please click ‘apply’ or contact Joe Pearce for any further information

About RBW Consulting

RBW Consulting is a life sciences talent & strategic consultancy with purpose, delivered through what we call Human Intelligence. We help life sciences businesses change the world by giving them the people, insight & networks to innovate and scale. We are proud of our role in helping companies deliver better health and wellbeing outcomes for patients We give back by playing an active role in funding initiatives that change lives We’ve created a culture rooted in support, transparency and mutual commitment. We lead with our values from the inside; empowering and investing in our people is more important than short-term commercial gain.

We are an equal opportunities Recruitment Business and Agency

RBW Consulting is an equal opportunity workplace. We prioritize talent (both current and potential) over resumes, challenge the status quo, and value people as our most important asset. We do not discriminate on the basis of race, ethnicity, colour, sex, gender identity or expression, sexual orientation, religion, age, marital status, visible or invisible disability, medical condition, national origin, veteran status, or any other protected status. We strive to be a diverse workforce that is representative at all levels and are committed to building a team that represents a variety of backgrounds, perspectives, and skills.

• Conduct pre-study, initiation, routine monitoring, and close-out visits to clinical trial sites.
• Verify the accuracy, completeness, and compliance of clinical data and source documents.
• Ensure that all study-related activities are conducted in accordance with the study protocol, Investigator's Brochure, and applicable regulations.
• Train and support investigators and site staff on study procedures and requirements.
• Monitor patient recruitment and retention at study sites.
• Identify, document, and escalate site issues and discrepancies to the Clinical Operations Manager.
• Ensure timely submission of study-related documents and regulatory information.
• Build and maintain positive relationships with clinical investigators and site personnel.
• Prepare and present monitoring visit reports.
• Participate in the development of study protocols and Case Report Forms (CRFs) as needed.

• Bachelor's degree in a life science, nursing, pharmacy, or related discipline; advanced degree preferred.
• Minimum of 3 years of experience as a Clinical Research Associate or equivalent role in the pharmaceutical or biotechnology industry.
• In-depth knowledge of GCP, ICH guidelines, and relevant regulatory requirements.
• Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS).
• Excellent understanding of medical terminology and clinical trial processes.
• Strong organizational, time management, and problem-solving skills.
• Exceptional written and verbal communication skills, with the ability to interact professionally with a variety of stakeholders.
• Ability to travel to clinical sites (approximately 50-70% travel may be required).
• Detail-oriented with a strong commitment to data integrity and patient safety.
• Proactive approach to identifying and resolving issues.

• Monitor clinical trial sites to ensure adherence to protocol, GCP, and regulatory requirements.
• Verify the accuracy, completeness, and consistency of clinical data.
• Manage study-related documentation and regulatory submissions.
• Communicate effectively with investigators, site staff, and study sponsors.
• Identify, evaluate, and select potential clinical trial sites.
• Train site personnel on study protocols and procedures.
• Perform site initiation, interim monitoring, and close-out visits.
• Address and resolve site-level issues and discrepancies.
• Ensure timely reporting of adverse events and protocol deviations.
• Contribute to the development of clinical trial protocols and study plans.

• Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
• Previous experience as a Clinical Research Associate or in a similar clinical research role.
• In-depth knowledge of Good Clinical Practice (GCP), ICH guidelines, and relevant regulatory requirements.
• Familiarity with clinical trial monitoring procedures and data management systems.
• Excellent organizational and time management skills.
• Strong attention to detail and accuracy.
• Effective written and verbal communication skills.
• Ability to travel to clinical sites as required.
• Proficiency in Microsoft Office Suite and clinical trial management software.
• A proactive approach to problem-solving and a commitment to patient safety.

• Plan, implement, and manage clinical trial activities at assigned sites.
• Conduct site initiation visits, interim monitoring visits, and close-out visits.
• Ensure compliance with Good Clinical Practice (GCP), regulatory guidelines, and study protocols.
• Verify the accuracy and completeness of clinical data through source data verification.
• Manage communication between the study sites and the sponsor organization.
• Identify and report adverse events and safety concerns promptly.
• Maintain essential study documents and site files.
• Train and support site staff on trial procedures and requirements.
• Monitor study progress and timelines, identifying and resolving potential issues.
• Contribute to the development of study protocols and case report forms.
• Prepare monitoring visit reports and follow up on action items.

• Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field; advanced degree preferred.
• Previous experience as a Clinical Research Associate or in a similar clinical trial role.
• Thorough understanding of ICH-GCP guidelines and regulatory requirements for clinical trials.
• Experience with clinical trial monitoring and data verification.
• Excellent organizational, time management, and problem-solving skills.
• Strong interpersonal and communication skills, with the ability to build rapport with site personnel.
• Proficiency in medical terminology and understanding of disease processes.
• Ability to travel to clinical sites as required (estimated at 40-60%).
• Proficiency in using clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
• A commitment to ethical research practices and patient safety.

• Perform site initiation, monitoring, and close-out visits in accordance with study protocols and regulatory guidelines.
• Ensure adherence to Good Clinical Practice (GCP), International Conference on Harmonisation (ICH) guidelines, and all applicable regulatory requirements.
• Verify the accuracy, completeness, and consistency of clinical data reported by investigators.
• Review and verify source documents against case report forms (CRFs).
• Manage and resolve data queries and ensure timely resolution of site issues.
• Oversee drug accountability and manage investigational product at study sites.
• Build and maintain strong working relationships with principal investigators, site staff, and other study stakeholders.
• Train site personnel on study procedures, protocol requirements, and regulatory compliance.
• Prepare monitoring visit reports and ensure follow-up actions are completed.
• Contribute to the development of study-related documents, including protocols, CRFs, and informed consent forms.
• Act as a key liaison between the sponsor, investigational sites, and regulatory authorities.
• Ensure patient safety and protocol compliance throughout the trial lifecycle.
• Participate in investigator meetings and provide essential study updates.
• Manage travel arrangements and submit expense reports in a timely manner.

• Bachelor's degree in a life science, nursing, or a related field.
• Proven experience as a Clinical Research Associate, with specific experience in oncology trials highly desirable.
• In-depth knowledge of ICH-GCP guidelines and regulatory requirements for clinical trials.
• Excellent understanding of medical terminology and clinical trial processes.
• Strong organisational, time management, and problem-solving skills.
• Exceptional attention to detail and accuracy.
• Proficient in the use of clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
• Excellent written and verbal communication skills.
• Ability to travel frequently to clinical sites (estimated 50-60% travel).
• Self-motivated, proactive, and able to work independently with minimal supervision.
• Commitment to ethical conduct and patient well-being.

• Job Title: Senior CRA / Senior CRA II
• Location: Remote in UK
• Salary: £50,000 - £58,000
• Additional Benefits: Car allowance (or company car) 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. We are seeking skilled monitors with a minimum of 3 years of CRA experience. 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; 3 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.

To apply

Please click ‘apply’ or contact Joe Pearce for any further information

About RBW Consulting

RBW Consulting is a life sciences talent & strategic consultancy with purpose, delivered through what we call Human Intelligence. We help life sciences businesses change the world by giving them the people, insight & networks to innovate and scale. We are proud of our role in helping companies deliver better health and wellbeing outcomes for patients We give back by playing an active role in funding initiatives that change lives We’ve created a culture rooted in support, transparency and mutual commitment. We lead with our values from the inside; empowering and investing in our people is more important than short-term commercial gain.

We are an equal opportunities Recruitment Business and Agency

RBW Consulting is an equal opportunity workplace. We prioritize talent (both current and potential) over resumes, challenge the status quo, and value people as our most important asset. We do not discriminate on the basis of race, ethnicity, colour, sex, gender identity or expression, sexual orientation, religion, age, marital status, visible or invisible disability, medical condition, national origin, veteran status, or any other protected status. We strive to be a diverse workforce that is representative at all levels and are committed to building a team that represents a variety of backgrounds, perspectives, and skills.