251 Research Associate 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.

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.

**Research Associate**
**Infrastructure Insights**
**Location:** UK or Ireland
**Work mode:** Home Based - Hybrid
**Position Summary:**
The **Research Associate - Infrastructure Insights** plays a key role in advancing Bentley's mission to inform and inspire positive change across the global infrastructure ecosystem. Sitting within the Infrastructure Policy & Advocacy (IPA) initiative, this role leads industry-insight monitoring and reporting for Bentley's leadership team.
You will design and manage a scalable research process to identify and track emerging trends in infrastructure markets, develop productive relationships with industry membership bodies, and deliver quarterly data-driven reports that help shape Bentley's strategic direction. This position offers the opportunity to collaborate across teams and ensure research outputs are accessible, inclusive, and aligned with Bentley's commitment to sustainability, innovation, and equity.
_Note: This role is internally titled_ **_Infrastructure Insights Lead_** _, reflecting its strategic scope and leadership responsibilities within the IPA initiative._
**Responsibilities:**
+ Lead the IPA's industry-insight monitoring and reporting function, developing a scalable process for market research and reporting that can grow across regions and business functions.
+ Conduct desk-based research and engage stakeholders - including industry associations and relevant bodies - to analyze:
+ Global developments across infrastructure sectors (transport, water, energy, etc.)
+ Infrastructure policy and investment trends in Bentley's key markets
+ Innovative funding, finance, and delivery models
+ Digital transformation trends in infrastructure
+ Synthesize research findings into quarterly insight reports, briefing notes, market scans, and landscape analyses to support Bentley's programs and partnerships.
+ Develop and maintain a knowledge base of relevant data sources, stakeholders, and industry initiatives, ensuring insights are accurate, timely, and broadly accessible to internal stakeholders.
+ Collaborate with cross-functional teams to support inclusive decision-making and knowledge sharing.
**Qualifications:**
+ Bachelor's degree in public policy, management, engineering, urban planning, economics, or a related field; Master's degree preferred but not required.
+ 5+ years of experience in research, consulting, or policy analysis, ideally within infrastructure or the built environment.
+ Strong analytical and critical thinking skills, with the ability to synthesize complex information into clear, actionable insights.
+ Excellent written and verbal communication skills in English (near-native fluency required); additional languages are a plus.
+ Self-starter with strong organizational skills, attention to detail, and a collaborative mindset.
+ Familiarity with infrastructure markets, public policy, and international business - or the ability to quickly learn and adapt.
+ Commitment to Bentley's values, including sustainability, innovation, and fostering an inclusive workplace.
+ We encourage candidates from diverse backgrounds to apply, even if you do not meet 100% of the listed qualifications.
**What We Offer:**
+ A great Team and culture - please see our colleague video .
+ An exciting career as an integral part of a world-leading software company providing solutions for architecture, engineering, and construction - watch this short documentary about how we got our start.
+ An attractive salary and benefits package.
+ A commitment to inclusion, belonging and colleague wellbeing through global initiatives and resource groups.
+ A company committed to making a real difference by advancing the world's infrastructure for better quality of life, where your contributions help build a more sustainable, connected, and resilient world. Discover our latest user success stories for an insight into our global impact.
**LI-BC #LI-Hybrid #LI-Remote**
 **About Bentley Systems**
Around the world, infrastructure professionals rely on software from Bentley Systems to help them design, build, and operate better and more resilient infrastructure for transportation, water, energy, cities, and more. Founded in 1984 by engineers for engineers, Bentley is the partner of choice for engineering firms and owner-operators worldwide, with software that spans engineering disciplines, industry sectors, and all phases of the infrastructure lifecycle. Through our digital twin solutions, we help infrastructure professionals unlock the value of their data to transform project delivery and asset performance. Opportunity Employer:**
Bentley is proud to be an equal opportunity employer and considers for employment all qualified applicants without regard to race, color, gender/gender identity, sexual orientation, disability, marital status, religion/belief, national origin, caste, age, or any other characteristic protected by local law or unrelated to job qualifications.
Equal Opportunity Employer/Minorities/Females/Veterans/Disabled

Our client, a leading global pharmaceutical company with a significant presence in London, England, UK , is seeking a highly qualified and meticulous Remote Clinical Research Associate (CRA) to support their groundbreaking research initiatives. This is a fully remote position, offering the opportunity to contribute to vital drug development from anywhere within the UK. You will be responsible for monitoring clinical trial sites, ensuring data integrity, and verifying compliance with regulatory requirements and study protocols. The ideal candidate possesses a strong scientific background, a thorough understanding of GCP guidelines, and exceptional organisational and analytical skills. This role is critical in ensuring the accuracy, validity, and timeliness of clinical trial data, contributing directly to the advancement of life-saving treatments.

Key responsibilities include:

• Performing remote site monitoring activities to ensure compliance with study protocols, SOPs, and GCP.
• Reviewing and verifying source documents, case report forms (CRFs), and electronic data capture (EDC) systems.
• Assessing the quality and integrity of data collected at clinical trial sites.
• Identifying and reporting potential protocol deviations and adverse events.
• Managing communication between study sites, investigators, and internal project teams.
• Ensuring site readiness for audits and regulatory inspections.
• Supporting site initiation, monitoring visits, and site closure activities.
• Maintaining accurate and up-to-date trial documentation and databases.
• Providing training and guidance to site staff on study-related procedures.
• Contributing to the development and review of study-related documents.

To be successful in this role, you must have a Bachelor's degree in a life science, nursing, or related field. A minimum of 3 years of experience as a Clinical Research Associate, with proven experience in remote monitoring, is essential. A comprehensive understanding of Good Clinical Practice (GCP) and regulatory guidelines (e.g., FDA, EMA) is mandatory. Excellent analytical, problem-solving, and communication skills are required, along with the ability to work independently and manage multiple priorities effectively. Proficiency with clinical trial management systems (CTMS) and EDC systems is expected. This is a fantastic opportunity for an experienced CRA to join a world-class organisation and play a key role in bringing innovative pharmaceutical products to market, all within a flexible remote working arrangement.

Our client is seeking a highly experienced and motivated Senior Clinical Research Associate (CRA) to join their dynamic pharmaceutical team based in London, England, UK . This role offers a hybrid working model, blending remote flexibility with essential on-site collaboration. As a Senior CRA, you will play a critical role in the planning, execution, and monitoring of clinical trials, ensuring adherence to protocols, regulatory requirements, and good clinical practice (GCP).

Key Responsibilities:

• 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.

Qualifications and Experience:

• 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.

This is an excellent opportunity for a seasoned CRA to take on greater responsibility and contribute significantly to groundbreaking pharmaceutical research in a supportive and innovative environment.

Our client, a leading global pharmaceutical company, is seeking a highly motivated and experienced Clinical Research Associate (CRA) to join their dynamic team. This role is essential for ensuring the successful execution of clinical trials in compliance with Good Clinical Practice (GCP) guidelines and regulatory requirements. You will be responsible for monitoring investigational sites, ensuring the quality and integrity of data collected, and verifying patient safety throughout the trial process. This hybrid role combines remote administrative tasks with on-site visits to clinical trial sites.

Key responsibilities include site selection, initiation, monitoring, and close-out visits. You will assess protocol adherence, verify source data, and ensure accurate and timely entry of data into clinical trial databases. Building and maintaining strong working relationships with investigators, site staff, and internal project teams is crucial. You will be responsible for resolving data queries, managing site supplies, and ensuring all regulatory documentation is up-to-date and accurately maintained. Adherence to study protocols, ethical principles, and company policies is paramount.

The ideal candidate will possess a Bachelor's degree in a life science, nursing, or a related field, with a minimum of 2-4 years of experience as a CRA or in a similar clinical research role. A thorough understanding of GCP, ICH guidelines, and regulatory requirements in the pharmaceutical industry is essential. Excellent communication, organizational, and time management skills are required, along with strong attention to detail and the ability to work independently. Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems is highly desirable. This role is based in the London, England, UK area, offering a hybrid working model that provides flexibility while ensuring necessary on-site engagement. If you are a dedicated professional committed to advancing medical research and patient care, we encourage you to apply.

Our client, a leading global pharmaceutical company, is seeking a dedicated and meticulous Clinical Research Associate (CRA) to join their fully remote clinical operations team. This crucial role involves overseeing and managing all aspects of clinical trials, ensuring compliance with regulatory standards, protocols, and ethical guidelines. As a remote CRA, you will conduct site visits (both pre-study, interim, and close-out), manage investigator sites, and ensure the quality and integrity of data collected. This is an excellent opportunity for experienced CRAs looking for a remote-first work environment with significant career growth potential.

Responsibilities:

• 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.

Qualifications:

• 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.

This position is a fully remote role, with travel expected for site visits, serving the London, England, UK region and beyond.

Our client, a leading innovator in the pharmaceutical sector, is seeking a highly experienced Senior Clinical Research Associate (CRA) to join their dynamic team in **London, England, UK**. This role offers a hybrid working model, blending the benefits of in-office collaboration with the flexibility of remote work.

As a Senior CRA, you will play a pivotal role in the planning, execution, and monitoring of clinical trials across various therapeutic areas. You will be responsible for ensuring that clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), Good Clinical Practice (GCP), and all applicable regulatory requirements. Your primary focus will be on site management, including site selection, initiation, monitoring, and close-out, ensuring data integrity and patient safety are paramount.

Key Responsibilities:

• 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.

Qualifications and Experience:

• 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.

This is an exceptional opportunity to contribute to groundbreaking research and advance your career in a supportive and forward-thinking environment. Join us in making a difference in patient lives.

Our client is a leading global pharmaceutical company dedicated to advancing cancer treatments. They are seeking a highly skilled and experienced Clinical Research Associate (CRA) specializing in Oncology to join their dynamic team. This role, based in the vibrant hub of London, England, UK , offers an exciting opportunity to contribute to critical oncology clinical trials, ensuring data integrity, patient safety, and adherence to regulatory guidelines. You will be a key player in bringing life-saving therapies to patients.

Responsibilities:

• 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.

Qualifications:

• 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.

This is a demanding but highly rewarding role for a dedicated professional. We offer a competitive salary, comprehensive benefits, and the opportunity to be at the forefront of cancer research.