263 Clinical Research Professionals jobs in London

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.

• Initiate, monitor, and close clinical trial sites, ensuring all trial activities are conducted according to the protocol, standard operating procedures (SOPs), and regulatory guidelines.
• Perform site visits, including pre-study, initiation, monitoring, and close-out visits, as required.
• Assess protocol compliance, including patient recruitment, informed consent process, and data accuracy.
• Ensure timely resolution of site issues and discrepancies.
• Train and mentor junior CRAs and site staff on protocol requirements and study procedures.
• Prepare and present study progress reports to project management and relevant stakeholders.
• Manage relationships with investigators, site staff, and other study vendors.
• Oversee drug accountability and investigational product management at trial sites.
• Ensure accurate and timely source data verification (SDV) and review of case report forms (CRFs).
• Contribute to the development and review of study-related documents, such as investigator brochures, protocols, and informed consent forms.
• Act as a key point of contact between the sponsor and the clinical trial sites.

• Bachelor's degree in life sciences, nursing, or a related field; advanced degree preferred.
• Minimum of 5 years of experience as a Clinical Research Associate in the pharmaceutical industry.
• In-depth knowledge of ICH-GCP guidelines, local regulatory requirements, and clinical trial processes.
• Proven experience in monitoring various phases of clinical trials.
• Strong understanding of medical terminology and disease areas relevant to pharmaceutical research.
• Excellent communication, interpersonal, and organizational skills.
• Ability to work independently and as part of a team, with a proactive and detail-oriented approach.
• Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
• Willingness to travel to sites as needed.

• Conduct pre-study, interim, and close-out visits to investigator sites according to protocol and regulatory requirements.
• Ensure compliance with Good Clinical Practice (GCP) guidelines, local regulations, and study protocols.
• Monitor study conduct and data quality at investigative sites through regular reporting and site visits.
• Verify the accuracy, completeness, and integrity of clinical trial data.
• Train and support site staff on study procedures, protocols, and regulatory requirements.
• Manage communication and relationships with investigators, site staff, and study sponsors.
• Ensure timely reporting of study progress, risks, and issues to project management.
• Oversee the initiation, maintenance, and termination of clinical sites.
• Manage the supply of study-related materials, including investigational products and trial supplies.
• Ensure the proper handling and archiving of all study-related documents.
• Participate in study team meetings and contribute to the overall success of the clinical trial.

• Proven experience as a Clinical Research Associate (CRA) or equivalent role in the pharmaceutical or biotechnology industry.
• Thorough knowledge of GCP, ICH guidelines, and regulatory requirements for clinical trials.
• Experience conducting site monitoring visits and managing multiple investigator sites.
• Strong understanding of clinical trial processes, from site initiation to study close-out.
• Excellent written and verbal communication skills, with the ability to build rapport with site personnel.
• Highly organized with exceptional attention to detail and ability to manage competing priorities.
• Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
• Ability to work independently and effectively manage your time in a remote setting.
• Valid driver's license and willingness to travel frequently for site visits.
• Bachelor's degree in a life science, nursing, or related field; advanced degree is a plus.
• Fluency in English is essential.

• Conduct site initiation visits to assess the feasibility of recruitment and ensure regulatory compliance.
• Perform routine monitoring visits (on-site and remote) to review source data, investigational product accountability, and regulatory documentation.
• Identify, evaluate, and resolve site-level issues and risks, escalating where necessary.
• Build and maintain strong relationships with investigators, study coordinators, and site staff.
• Ensure timely and accurate submission of all required study-related documentation.
• Train and mentor junior CRAs, providing guidance and support.
• Contribute to the development and review of study protocols and other essential documents.
• Participate in the preparation of site audit readiness and respond to audit findings.

• Bachelor's degree in life sciences, nursing, or a related field; advanced degree preferred.
• Minimum of 5 years of experience as a Clinical Research Associate in the pharmaceutical or biotechnology industry.
• Thorough understanding of ICH-GCP guidelines and relevant regulatory requirements.
• Proven experience in monitoring multiple clinical trials simultaneously.
• Excellent communication, interpersonal, and problem-solving skills.
• Ability to work independently and manage time effectively.
• Proficiency in electronic data capture (EDC) systems and other clinical trial management software.
• Willingness to travel up to 50% of the time within the assigned territory.

• Monitor clinical trial sites to ensure compliance with protocol, SOPs, GCP, and regulatory requirements.
• Perform site initiation, interim, and close-out monitoring visits.
• Verify accuracy and completeness of clinical data through source data verification (SDV).
• Identify, evaluate, and recommend potential investigators and study sites.
• Manage study site relationships, providing training and ongoing support to investigators and study staff.
• Ensure timely submission of required documentation and reports.
• Track study progress, identify risks, and implement corrective actions to ensure milestones are met.
• Manage investigational product accountability and drug reconciliation.
• Oversee patient recruitment and retention efforts at study sites.
• Prepare monitoring visit reports and communicate findings and recommendations to study teams and sites.
• Ensure all regulatory and ethical guidelines are followed throughout the trial lifecycle.
• Participate in study team meetings and contribute to protocol development where applicable.
• Maintain effective communication with internal and external stakeholders.
• Manage site budgets and payments as required.
• Contribute to the development of monitoring plans and risk-based monitoring strategies.
• Ensure timely resolution of data queries and discrepancies.
• Uphold the highest standards of patient safety and data integrity.
• Stay current with advancements in oncology research and clinical trial methodology.
• Contribute to the training and mentoring of junior CRAs.

• Bachelor's degree in a life science, nursing, pharmacy, or related discipline. An advanced degree is a plus.
• Minimum of 3-5 years of independent clinical monitoring experience, with a strong emphasis on oncology trials.
• In-depth knowledge of ICH-GCP guidelines and regulatory requirements for clinical trials.
• Proven ability to conduct site visits, review data, and ensure compliance.
• Excellent understanding of oncology disease states and treatment paradigms.
• Strong analytical and problem-solving skills.
• Exceptional written and verbal communication abilities.
• Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
• Ability to travel frequently (up to 60%) within the UK and potentially internationally.
• Strong organizational skills and the ability to manage multiple priorities effectively.
• A professional and proactive attitude with a commitment to quality.
• Ability to work independently and as part of a cross-functional team.
• Experience with rare disease or early-phase oncology trials is an advantage.