Overview In this remote, senior role you shape and govern clinical data standards within oncology trials in a CRO setting. You will lead the development and implementation of data standards, ensuring regulatory alignment and CDISC complianc...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 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>>.

Overview As a Senior Clinical Research Associate, you will help build and shape Quotient Sciences' clinical monitoring function across early-phase trials. You will partner with Clinical Operations, Quality Assurance and study teams to uphol...Read More>>.

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 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 global non-interventional studies as a Senior Lead CRA, guiding cross-country teams to ensure high-quality site management and compliance. You collaborate with Sponsors, PMs, and regulators to advance study s...Read More>>.

Overview In this Senior CRA role, you will lead site management, monitoring, and close-out for investigator sites in alignment with the Study Monitoring Plan and GCP. You’ll drive trial activities from activation to database lock, ensurin...Read More>>.

Overview In this role you support the execution of interventional studies as a Clinical Research Associate within IQVIA's sponsor-dedicated team. You will conduct on-site monitoring and ensure compliance with GCP/ICH while collaborating wit...Read More>>.

Overview As a CRA II in the UK, you monitor and manage clinical site performance to ensure regulatory and protocol compliance. You will work within the Clinical Solutions group, collaborating with cross-functional teams to support data qual...Read More>>.

Overview In this Senior CRA role, you will oversee site management, monitoring, and close-out for assigned investigative sites to safeguard patient safety and ensure high-quality study execution. You’ll manage operational activities from...Read More>>.

Overview In this Senior CRA role, you will lead and execute site-centric activities to deliver high-quality clinical studies for a key sponsor. You will collaborate with local study teams to ensure patient safety, regulatory compliance, and...Read More>>.

Get AI-powered advice on this job and more exclusive features.Direct message the job poster from EPM ScientificConsultant at EPM Scientific | Permanent SolutionsWe're currently partnering with a leading international pharmac...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>>.

Closing date: Friday 11th September 2026 The Bank Clinical Research Study Coordinator will play a key role in supporting the delivery of high-quality clinical trials across the Northwest. Based within EMS' mobile and fixed-site research...Read More>>.

IQVIA LLC is seeking a site-based Clinical Research Associate to manage monitoring activities and ensure regulatory compliance across trials in Leeds. You will track submissions, site recruitment, data queries and documentation, while maintaining...Read More>>.

IQVIA is seeking an experienced Clinical Monitoring professional to oversee site visits and ensure protocol adherence across multiple sites in the United States. You will drive recruitment planning and manage regulatory submissions while maintaini...Read More>>.

Durham, North Carolina, United States of America Aurora, Illinois, United States San Fernando, California, United States Clinton, Missouri, United States Mansfield, Ohio, United States Santa Cruz, California, Uni...Read More>>.

We are looking to recruit an experienced dedicated Senior Clinical Research Nurse to join the Research and Innovation department at Frimley Health NHS Foundation Trust. The post holder will work with a vibrant team of research nurses and practi...Read More>>.

Job Title: Research Associate in the Digital Validation of Engineered Porous Structures, LoughboroughApplication Closing Date: Sunday, 11 October 2026...Read More>>.

Job Title: Research Associate in Metal Additive Manufacturing, LoughboroughApplication Closing Date: Sunday, 18 October 2026We are seeking a high...Read More>>.

Join IQVIA on our mission to accelerate innovation for a healthier world! IQVIA UK’s cFSP (sponsor-dedicated) team is growing and seeking experienced Clinical Research Associates. Why IQVIA?...Read More>>.

Join Us on Our Mission to Drive Healthcare Forward IQVIA cFSP (sponsor-dedicated) are seeking experienced Clinical Research Associates in the UK. With access to world-class training and professional development, we’ll give you t...Read More>>.

Postdoctoral Research Associate - Durham The Role and DepartmentApplications are invited for a Postdoctoral Research Associate (PDRA) in experimental earthquake mechanics to join the N...Read More>>.

Freelance CRA – UK | French & English Speaking I’m currently supporting a CRO looking to bring an experienced Freelance CRA onto a part-time, sponsor-dedicated project. The CRA will be based in the UK and work closely with b...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>>.

ARC Regulatory in Belfast is seeking a Clinical Research Associate to monitor in vitro diagnostic device clinical sites, ensuring compliance with the study protocol, ICH GCP, and local regulations. The role involves site qualification, initiation,...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>>.

Pulse Healthcare in Manchester is seeking a dedicated Clinical Research Physician to join our team in the North West. The role involves conducting clinical trials, ensuring regulatory compliance, and advancing medical knowledge.Flexible, of...Read More>>.

Parexel FSP is seeking an experienced Senior CRA to join a large Sponsor’s EU project. The role focuses on site management, monitoring and close-out of investigator sites to ensure patient safety and high-quality study execution.Key respo...Read More>>.

Parexel FSP is hiring for an experienced Senior CRA level to join one of our large Sponsor’s in the EU. Some specifics about this advertised role This role is responsible for the site management, site monitoring and close-out o...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>>.

ICON Strategic Solutions, part of ICON, invites a Senior Clinical Research Associate to join sponsor-dedicated model, supported by ICON’s global expertise. As CRA II, you will design and analyse trials, interpret data, and contribute to developm...Read More>>.

We are seeking a dedicated and motivated Clinical Research Physician to join our Early Phase Clinical Unit (EPCU) in London. This is an exciting opportunity to play a pivotal role in early-phase clinical research, contributing to the development o...Read More>>.

Research Associate in Mineral Construction Materials (SB13933) - Bath, BA2 7AYAbout the roleThe role is part of an exciting partnership with the University of Malaga in Spain, University of Manchester in the UK, and the European...Read More>>.

Research Associate (SB13960) - Bath, BA2 7AYAbout the roleAdvance Your Engineering Career Through Innovation and ImpactThe...Read More>>.

Research Associate in Spectroscopy and Molecular Modelling for Zeolite Catalysed Alcohol-to-jet-fuel Catalysis (SS13564R) - Bath, BA2 7AYAbout the roleThis role is part of the UK Catalysis Hub where the practical...Read More>>.

Research Associate/Fellow in Engineered Silk Manufacturing and Optical Fibre Technologies (SS13969) - Bath, BA2 7AYAbout the roleJoin the HOLLOW SILK project, an ambitious research project funded b...Read More>>.

Junior User Researcher - Associate Consultant - Digital Excellence - LondonReference Code: 350231-en_GBContract Type:PermanentProfessional Communities: Strategy & Transformation....Read More>>.

Clinical Research AssociateLocation: Belfast / Travel requiredJob Purpose:Act in the role of clinical site monitor to regularly visit/remotely assess in vitro di...Read More>>.

University of Cambridge is seeking a Research Associate (Honorary Resident Doctor) to join our paediatric diabetes research programme. You will contribute to trials and translational studies, aiming to improve outcomes for children with Type 1 Dia...Read More>>.

Oxford Health's NIHR Clinical Research Facility (CRF) in Oxford is seeking a Recruitment Facilitator on a secondment basis. You will provide specialist recruitment expertise to support complex commercial and early-phase studies, working with resea...Read More>>.

The Acute Multidisciplinary Imaging and Intervention Centre (AMIIC) at the University of Oxford, within the John Radcliffe Hospital, Oxford, invites applications for a 2-year Apprentice Research Administrator role. The programme offers on-the-job...Read More>>.

Salary: £51,931 per annum, the starting salary is determined by relevant clinical experience Reporting to: Edward Johnston Duration ofContract: 2 years in the first instance with the possibility of extension....Read More>>.

Manchester University NHS Foundation Trust is seeking a Quality Assurance professional to join the Quality Team, supporting QA activities across the Clinical Research Facilities (CRF) at MFT. The post holder will conduct audits, maintain quality m...Read More>>.

OverviewVelocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites. At Velocity, we align our values and behaviors to give...Read More>>.

Thermo Fisher Scientific's PPD FSP division is seeking a Clinical Research Associate to support multinational clinical monitoring projects. You will perform on-site monitoring, ensure quality and compliance with ICH-GCP, EU and FDA requirements, a...Read More>>.

Thermo Fisher Scientific, through its PPD clinical research services, is seeking an experienced Assistant Clinical Research Associate (ACRA) to join our UK team. You will perform remote activities, support site management and monitoring processes,...Read More>>.