Overview In this role you drive quality-driven clinical monitoring for investigator sites, ensuring studies run per protocol and regulatory standards. You work closely with sponsors and cross-functional teams, coordinating start-up, initiat...Read More>>.

Overview In this role you will support the advancement of clinical development by conducting on-site monitoring and oversight of trial activities. You’ll collaborate with sites to ensure protocol adherence, data integrity, and regulatory...Read More>>.

Overview As a CRA at Parexel, you will go beyond traditional monitoring to safeguard patient wellbeing and ensure study success across UK sites. You’ll manage site relationships, oversee quality from site identification to close-out, and...Read More>>.

Overview In this evergreen role, you contribute to a closely aligned sponsor partnership within a collaborative, quality-driven environment. You will monitor and support clinical studies at investigative sites, ensuring compliance with prot...Read More>>.

Overview In this role you drive site monitoring across interventional studies, ensuring GCP/ICH compliance and high-quality data. You collaborate with sites to optimize subject recruitment and manage study documentation. You’ll track regu...Read More>>.

Overview You will support and oversee clinical studies from a home-based role in the UK or Northern Ireland, ensuring studies are conducted to protocol, SOPs, and ICH-GCP standards. You will coordinate study setup and monitoring activities,...Read More>>.

Overview As a Clinical Research Associate in Abbott Diabetes Care, you contribute to advancing diabetes care through clinical studies supporting innovative medical technologies. You’ll join a collaborative Clinical Affairs team in Witney,...Read More>>.

Overview In this role you will monitor clinical studies across investigative sites, ensuring adherence to protocol, SOPs, ICH-GCP, and applicable regulations. You will coordinate study setup and monitoring activities, including investigator...Read More>>.

Join to apply for the Senior Clinical Research Associate role at TFS HealthScience3 weeks ago Be among the first 25 applicantsJoin to apply for the Senior Clinical Research Associate...Read More>>.

Lead Clinical Research Nurse Who are we? Clerkenwell Health is an innovative and leading Research Organisation specialising in the delivery of scientifically grounded clinical trials through its collaborative Contract Res...Read More>>.

1 day ago Be among the first 25 applicantsGet AI-powered advice on this job and more exclusive features.Our client, an international clinical research organisation (CRO) is currently looking for a Senior Clinical Research Phy...Read More>>.

Job Summary We are seeking a Medical Director – Oncology/Solid tumor to join our dynamic team. The Medical Director will have overall responsibility for providing medical, scientific, and strategic leadership for the successful plann...Read More>>.

Act in the role of clinical site monitor to regularly visit/remotely assess in vitro diagnostic medical device clinical study sites and ensure that the study is conducted in compliance with the study protocol, ICH GCP and local regulatory requi...Read More>>.

We are seeking a dedicated Clinical Research Physician to join our team in the North West. The ideal candidate will be involved in conducting clinical trials, ensuring they meet regulatory standards while advancing medical knowledge. This role...Read More>>.

Clinical Research AssociateLocation: Belfast / requires travel when requiredJob Purpose:Act in the role of clinical site monitor to regularly visit/remotely assess in vitro diagnostic medical device clinical study sit...Read More>>.

Senior Clinical Research Associate / Clinical Study ManagerSouthampton, Hampshire, United Kingdom (Sur site)Job DescriptionJob title: Senior Clinical Research Associate / Clinical Study ManagerDepartment:...Read More>>.

Syneos Health is seeking a Senior CRA with UK monitoring experience to perform site qualification, initiation, monitoring, and close-out visits in a fast-paced, globally integrated environment. The role involves on-site and remote activities, ensu...Read More>>.

Single Sponsor Senior Clinical Research Associate (UK monitoring experience needed) Updated: Today Location: Remote, LND, United Kingdom Description Single Sponsor Senior Clinical Research Associate (U...Read More>>.

School/Department: School of Medicine & Population Health Work Arrangement: Full Time (Hybrid) Contract Type: Fixed-term Closing Date: 28/10/2026 The University of Sheffield is a remarkable place to work. Our people are...Read More>>.

A leading CRO are looking for a Clinical Research Coordinator in London, UK.This is an exciting opportunity with candidates to start as soon as possible and great opportunity to gain industry experience.The Clini...Read More>>.

The University of Sheffield is a remarkable place to work. Our people are at the heart of everything we do. Their diverse backgrounds, abilities and beliefs make Sheffield a world-class university. We offer a fantastic range of benefits inc...Read More>>.

Senior/Lead Clinical Research Associate (CRA) - Remote in the United KingdomAre you an experienced CRA looking for your next significant step? Do you thrive in an environment that values a thoughtful approach to site management and p...Read More>>.

ICON Clinical Research is seeking a Senior Clinical Research Associate (CRA) to oversee and manage clinical trial activities within the Full-Service team in the UK. The role focuses on data integrity, regulatory compliance, and patient safety acro...Read More>>.

Oncology Clinical Researcher (AI Training) About The Role What if your deep knowledge of cancer clinical trials could directly shape how AI reasons about one of medicine's most complex and high-stakes fields? We're looking for an...Read More>>.

Senior Clinical Research Associate (CRA) Location: Bridgend, Scotland, United Kingdom Work Arrangement: Site-based monitoring with travel to clinical trial sites Employment Type: Not specified Role...Read More>>.

Our Clinical Operations (multi-sponsor) team in the UK is looking for a passionate CRA I with at least 6 months of independent monitoring experience to work across a diverse range of therapeutic areas – including Hematology/Oncology and Ophthalm...Read More>>.

Syneos Health is seeking a Senior Clinical Research Associate with UK monitoring experience to oversee site qualification, initiation, monitoring and close-out visits, ensuring GCP compliance and patient safety across trials. The role requires up...Read More>>.

IQVIA is seeking an experienced Senior Clinical Research Associate to monitor and manage sites in the UK, ensuring protocol compliance and data quality. You will perform site visits, train sites, and collaborate with study teams to keep projects o...Read More>>.

Abbott in the United Kingdom is seeking a Clinical Research Associate to support the delivery of clinical studies, ensuring activities align with study protocols, GCP, SOPs and regulatory requirements.You will develop relationships with cli...Read More>>.

IQVIA in the United Kingdom seeks experienced Clinical Research Associates to monitor trials and ensure sites conduct studies according to the protocol and regulatory requirements. The role involves site visits, recruitment tracking, protocol trai...Read More>>.

R&D Partners is seeking a Clinical Research Associate to coordinate and oversee clinical studies in the UK. You will act as the primary contact for study sites, support site activation, and collaborate with cross-functional teams to ensure success...Read More>>.

Are you ready to drive the future of clinical research? Looking to be in the heart of a company where precision meets purpose? R&D Partners is seeking a Clinical Research Associate to join our team. In this role, you will coordinate and ove...Read More>>.

Abbott in the United Kingdom is seeking a Clinical Research Associate to support the delivery of clinical studies, ensuring compliant conduct, documentation and reporting in line with GCP, SOPs, and regulatory requirements.You will develop...Read More>>.

IQVIA LLC is seeking an on-site Clinical Research Associate to monitor trial sites, ensure protocol compliance and maintain regulatory documentation. The role involves coordinating site activation, ongoing monitoring, and data query resolution acr...Read More>>.

IQVIA is seeking an on-site Clinical Research Associate to support site monitoring across multiple sites in the United Kingdom. You will conduct monitoring visits, ensure GCP compliance, and manage essential trial documentation with the study team...Read More>>.

IQVIA LLC is seeking an on-site monitoring professional to ensure adherence to GCP and protocol requirements across multiple sites. You will manage site communications, training, and issue resolution while tracking regulatory submissions and data...Read More>>.

Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH)...Read More>>.

IQVIA LLC is seeking experienced Clinical Research Associates in the UK to monitor study sites and manage site activities in line with the protocol and regulatory requirements.Responsibilities include site visits, regulatory tracking, and m...Read More>>.

Are you looking to build a career as a Clinical Research Associate within a specialist clinical research environment where you can develop your expertise, gain greater autonomy, and make a genuine impact? Our client is a privately owned, sp...Read More>>.

RBW Consulting in London seeks a Clinical Research Associate to join a specialist CRO environment. You will monitor studies, ensure compliance with GCP, and support site management with investigators and staff.The role offers focused work w...Read More>>.

IQVIA UK is seeking an experienced Clinical Research Associate for the South West England region. The role involves on-site monitoring visits, protocol training, and collaboration with study teams to ensure regulatory compliance and data integrity...Read More>>.

Join IQVIA on our mission to accelerate innovation for a healthier world! IQVIA UK’s Site Management (multi-sponsor) team is growing and seeking experienced Clinical Research Associates. We are recognised as a 2026 "Glassdoo...Read More>>.

An exciting opportunity has arisen for a Band 6 Clinical Research Nurse post within the GI and Lymphoma Unit. The post holder will be working in the GI and Lymphoma unit Unit at the Royal Marsden NHS Foundation Trust based at Sutton. We are a high...Read More>>.

Industry: Clinical Research / Life SciencesFunction: Clinical Operations / ResearchAbout the RoleSeeking a Clinical Research Associate to support Oncology clinical trials across UK sites. The role involves indepe...Read More>>.

An opportunity has arisen for a Clinical Research (Nurse) Practitioner at Mersey Care NHS Foundation Trust. The post holder will be responsible for the delivery of a portfolio of clinical research studies delivered across the Mersey Care NHS Found...Read More>>.

Clinical Operations (multi-sponsor)Our team in the UK is looking for a passionate CRA I with at least 6 months of independent monitoring experience to work across a diverse range of therapeutic areas – including Hematology/Onc...Read More>>.

Abbott is seeking a Clinical Research Associate to join its Clinical Affairs team in Witney. This role offers hands-on experience in monitoring clinical studies and contributing to innovative diabetes care technologies.The successful candid...Read More>>.

Main area Research Grade Band 5 Contract Fixed term: 12 months (12 months from start date) Hours Full time - 37.5 hours per week Job ref 350-TWS8249391-A Employer Mersey Care NHS Foundation Trust Employer type NHS Site Hollins Park Hospital...Read More>>.

Standard Office Hours (40/wk)Environmental Conditions Able to lift 40 lbs. without assistance, Cold Room/Freezers -22degreesF/-6degrees C, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab co...Read More>>.