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>>.

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>>.

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>>.

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>>.

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>>.

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>>.

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>>.

We are recruiting two Senior Clinical Research Nurses to join our established research teams: one in Haematology and one in Lymphoma. These roles offer the opportunity to deliver a diverse and expanding portfolio of clinical trials in haematologic...Read More>>.

University Hospitals of North Midlands NHS Trust invites applications for a Clinical Research Matron/Delivery Manager. Lead a high-performing research delivery team within the Research & Innovation Directorate to grow impactful clinical research t...Read More>>.

Syneos Health is seeking a Senior CRA - Oncology for UK-based on-site and risk-based monitoring. The role requires monitoring expertise, strong regulatory knowledge, and the ability to lead site activities while supporting cross-functional teams t...Read More>>.

NHS Medical & Dental: Clinical Research FellowMain area Clinical Research Grade NHS Medical & Dental: Clinical Research Fellow Contract 12 months (Fixed term for 12 months with the possibility of extension) Hours Full time - 40 hours per...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>>.

The post holder will lead and develop the research delivery service, overseeing the delivery and coordination of a portfolio of clinical research studies from feasibility to archiving. They will ensure that all research undertaken safeguards the w...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 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>>.

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>>.

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>>.

Diversity and Inclusion Statement Mersey Care NHS Foundation Trust celebrates diversity and promotes equal opportunities; we are committed to challenging and eliminating racism and other forms of discrimination and advancing and promoting...Read More>>.

The University of Manchester is seeking a motivated Clinical Research Associate on a fixed-term, part-time contract to lead innovative studies into schizophrenia and related disorders, employing fMRI, EEG biomarkers and other experimental medicine...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 North West Regional Research Delivery Network (NW RRDN) is seeking a motivated and enthusiastic Clinical Research Practitioner for the Cheshire and Merseyside region. This role offers the opportunity to work across a range of health and care s...Read More>>.

We are seeking an enthusiastic Clinical Research Nurse to join our team at our clinical trials unit based in Glasgow. Supported by our fully trained clinical research team you would have responsibility for the care and wellbeing of our tria...Read More>>.