1,462 Clinical Positions 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.

• Design and develop clinical trial protocols in accordance with scientific objectives and regulatory requirements.
• Oversee the execution of clinical trials, ensuring compliance with ICH-GCP and other relevant regulations.
• Manage study timelines, budgets, and resources effectively.
• Collaborate with investigators and clinical site staff to ensure high-quality data collection.
• Analyze and interpret clinical trial data, contributing to study reports and publications.
• Prepare study-related documents, including investigator brochures, case report forms, and regulatory submission dossiers.
• Liaise with regulatory authorities and ethics committees.
• Contribute to the scientific strategy for drug development programs.
• Mentor and guide junior research staff.

• PhD or Master's degree in Life Sciences, Pharmacy, Medicine, or a related field.
• Minimum of 5 years of experience in clinical research and development within the pharmaceutical industry.
• Thorough understanding of clinical trial design, execution, and data analysis.
• In-depth knowledge of ICH-GCP guidelines and regulatory submission processes.
• Excellent scientific writing, analytical, and problem-solving skills.
• Strong interpersonal and communication skills, with the ability to build effective relationships.
• Experience in (Specific Therapeutic Area, e.g., Oncology, Cardiology) is a plus.
• Proficiency in relevant clinical trial management systems and statistical software.

• 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.

• Recruit, screen, and enroll eligible participants for clinical trials.
• Obtain informed consent from participants, ensuring they understand the study procedures, risks, and benefits.
• Collect, manage, and process study data accurately and efficiently, maintaining case report forms (CRFs) and electronic data capture (EDC) systems.
• Monitor participants' progress throughout the trial, documenting any adverse events or deviations from protocol.
• Ensure compliance with Good Clinical Practice (GCP) guidelines, FDA regulations, and other relevant ethical and regulatory standards.
• Schedule and coordinate participant appointments, laboratory tests, and other study-related procedures.
• Maintain accurate and organized study files, including essential documents, regulatory binders, and source documentation.
• Liaise with investigators, study sponsors, contract research organizations (CROs), and Institutional Review Boards (IRBs)/Ethics Committees.
• Assist in the preparation of study protocols, amendments, and reports.
• Manage study supplies and equipment, ensuring their availability and proper functioning.
• Participate in study initiation, monitoring, and close-out visits.
• Contribute to a safe and efficient research environment.

• Bachelor's degree in a life science, nursing, or related healthcare field.
• Previous experience working as a Clinical Research Coordinator or in a similar clinical research role is required.
• In-depth knowledge of GCP guidelines, clinical trial processes, and regulatory requirements.
• Experience with EDC systems and clinical data management is essential.
• Excellent organizational, time management, and multitasking abilities.
• Strong interpersonal and communication skills, with the ability to interact effectively with participants, healthcare professionals, and sponsors.
• Proficiency in Microsoft Office Suite.
• Attention to detail and commitment to accuracy.
• Ability to work independently and as part of a team in a fast-paced research setting.
• Certification as a Clinical Research Professional (e.g., SoCRA, ACRP) is a significant advantage.

• 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.