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 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>>.

China Development Center seeks individuals to support and conduct clinical research in China. One of the most critical missions of clinical research in China is to shorten the gap in drug lag so that effective treatment options become available to...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>>.

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>>.

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>>.

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>>.

A leading global clinical research organization is seeking experienced physicians to join its growing clinical development team in the UK. This position offers the opportunity to play a key role in the delivery of clinical trials, either as a S...Read More>>.

We have an exciting opportunity for an experienced Clinical Research Matron/Clinical Research Delivery Manager to join the Research and Innovation Directorate at University Hospitals of North Midlands NHS Trust (UHNM). This role is central to adva...Read More>>.

Job Description Job title: Senior Clinical Research Associate / Clinical Study Manager Department: Research & Development Location: Southampton, UK GLS: T03 Working hours: 37.5 hours per week Monday to Friday (...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>>.

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>>.

that support innovative healthcare technologies used globally.Main ResponsibilitiesAs a Clinical Research Associate, you will support the delivery of clinical studies, helping to ensure they are conducted, documented, and reported in accordance wi...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>>.

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>>.

IQVIA cFSP (sponsor-dedicated) invites applications for a Research Associate in Oncology. The role involves on-site monitoring across UK sites, ensuring GCP/ICH compliance, and coordinating with study teams. Training and professional development a...Read More>>.

Clinical Research Practitioner/ Clinical Research NurseBand 6Main area Cancer Grade Band 6 Contract 1 year (Fixed Term: 1 year) HoursFull timePart timeFlexible working37.5 hours per week (F...Read More>>.

The post holder will be a key member of the clinical research team. They will assist in the management, co-ordination and facilitation of clinical trial activities to support delivery of current and future studies inthe research team to tim...Read More>>.

Job summary This is an exciting role which will offer candidates the opportunity to continue to work in a clinical environment whilst also developing their research skills. The post holder will be part of a multidisciplinary team includin...Read More>>.

We are seeking a motivated and collaborative individual to join our team as a Clinical Research Associate. This fixed-term, part-time role will undertake innovative studies of the causes of schizophrenia and related disorders, including studies te...Read More>>.

The University of Manchester is seeking a Clinical Research Associate for a fixed-term, part-time role to support studies on schizophrenia and related disorders. The post involves cutting-edge techniques including fMRI and EEG biomarkers, with gov...Read More>>.

The University of Manchester is seeking a clinically oriented Research Associate to support innovative schizophrenia studies using fMRI, EEG biomarkers and related research methods. This fixed-term, part-time role focuses on advancing experimental...Read More>>.

Job summary An 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. Main duties of the job Please note for...Read More>>.