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 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 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>>.

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>>.

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>>.

Job Title: Research Associate in Regenerative Design Research, LoughboroughApplication Closing Date: Monday, 12 October 2026Loughborough Universi...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>>.

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>>.

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>>.

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>>.

The Department of Surgery and Cancer at Imperial College would like to recruit a Clinical Research Fellow to start in October/November 2026 within the Translational Colorectal Research Laboratory (https://www.imperial.ac.uk/department-surgery-canc...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>>.

Research Associate (SS13981) - Bath, BA2 7AYAbout the roleThe role is associated with the Royal Society International Collaboration Award “Operator learning for gradient flows with applications in imaging” led b...Read More>>.

Postdoctoral Research Associate (SS13987) - Bath, BA2 7AYThe Department of Mathematical Sciences at the University of Bath welcomes applications for an EPSRC-funded Research Associate in Analysis to work with Dr Matthew Schrecker in nonl...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>>.

IQVIA is seeking a Senior Clinical Research Associate (cFSP sponsor-dedicated) in Reading to monitor sites and manage study data per protocol and GCP. You will coordinate monitoring visits, support recruitment plans, and ensure regulatory complian...Read More>>.

MSD is seeking a motivated Clinical Research Associate (CRA) to join our clinical operations team. The CRA serves as the primary site contact and site manager throughout all study phases, ensuring high-quality trial execution and compliance with I...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>>.

Clinical Research AssociateDepartment: Corporate ServicesEmployment Type: Fixed Term - Full TimeLocation: RemoteCompensation: £28,560 / yearDescriptionPriory are looking to...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>>.

IQVIA UK's cFSP (sponsor-dedicated) team is growing, seeking experienced Clinical Research Associates to monitor interventional studies in the UK. You will perform site visits, support recruitment strategies, train site staff, and ensure regulator...Read More>>.

IQVIA UK invites applications for Clinical Research Associates (CRAs) to join our Site Management team in Manchester. You will conduct site monitoring visits, support recruitment plans, ensure GCP/ICH compliance, and maintain TMF documentation....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>>.

IQVIA in the United Kingdom seeks experienced Clinical Research Associates to monitor and manage study sites, ensuring adherence to protocol, GCP/ICH guidelines, and regulatory requirements. The role involves site visits, recruitment support, trai...Read More>>.

Overview Velocity 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>>.

Overview Velocity 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>>.

To conduct research in NIHR portfolio studies in the priority area of: Cardiovascular disease.Excellent opportunity for a resident doctor interested in 12 months of full-time cardiovascular research activities at Lancashire Cardiac Centre,...Read More>>.

Research Associate - ABACWS, CardiffResearch Associate...Read More>>.

Research Associate - Tower Building, CardiffResearch AssociateWe are seeking a Research Associate to join a UKRI Future Leaders Fellowshi...Read More>>.

Research Associate (Behaviour Change & Co-production) - Neuadd Meirionnydd, CardiffResearch Associate (Behaviour Change and Co-production)Centre for Trials Research (CTR)College of Biom...Read More>>.