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>>.

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>>.

Tigermed is seeking an experienced CRA to oversee site management, training, documentation, safety reporting, finance, and tool maintenance across multiple studies. The role requires in-depth knowledge of ICH-GCP and clinical trial operations, wit...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>>.

Company Description About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable...Read More>>.

AbbVie seeks a field-based Clinical Research Associate (CRA) to advance AbbVie's pipeline by partnering with study teams, internal R&D stakeholders, investigators and site staff. You will ensure trial conduct, data integrity and patient safety whi...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>>.

This is an exciting opportunity 12 month fixed-term contract for a clinician at higher speciality training level ST4-6 or equivalent, who is seeking to join a dynamic and expanding research team at Kent and Medway Mental Health NHS Trust. The post...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>>.

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>>.

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>>.

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>>.

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 and manage study sites, ensuring adherence to protocol, GCP/ICH guidelines, and regulatory requirements. The role involves site visits, recruitment support, trai...Read More>>.

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therap...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>>.

The Cambridge-GSK Translational Immunology Collaboration (CG-TIC) invites applications for a Research Associate (Honorary Resident Doctor) based in the Department of Medicine, Cambridge. You will conduct high-quality clinical and laboratory studie...Read More>>.

Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions...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>>.

Norwich Clinical Trials Unit at the University of East Anglia is seeking a Research Associate to support high-quality clinical statistics delivery within the Norwich Clinical Trials Unit.The role involves working with a Senior Statistician...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>>.

City St George’s, University of London is the University of business, practice and the professions and brings together the expertise and excellence of City, University of London and St George’s, University of London into one institution....Read More>>.

Clinical Research Nurse – Band 6 – HIV Research We are looking for a motivated and enthusiastic nurse to join the HIV Research Team at the Harrison Wing, Guy's and St Thomas Foundation Trust. The successful candidate will...Read More>>.

Job OverviewAn exciting opportunity has arisen for a Clinical Research Officer Band 5 to work as part of the Health and Care Research Wales Research and Development team in the BCUHB.Job OverviewAn exci...Read More>>.