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>>.

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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>>.

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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 will support clinical research at the frontline, coordinating with project stakeholders to meet timelines, targets and data quality standards. You will nurture relationships with clinical sites and investigators, w...Read More>>.

Overview As a Clinical Research Physician in Parexel's EPCU London, you provide medical oversight for early-phase trials, safeguarding participant safety and data integrity while ensuring regulatory compliance. You collaborate with cross-fu...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>>.

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>>.

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>>.

Main area Research Grade Speciality Doctor Contract Permanent Hours Full time - 40 hours per week (Evening, weekend and bank holiday on call) Job ref 370-MEDSDCR-1584-AEmployer North Cheshire and Mersey NHS Foundation Trust Employer type NH...Read More>>.

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

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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 postholder will be embedded in the project team and will have access to a home academic discipline within the University. The post-holder's line manager will be Helen Cra...Read More>>.

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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>>.

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>>.

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 Future Health is seeking a Research Access Reviewer to lead scientific and technical reviews of proposals for data, samples and participant access. You will work with the Access Board and researchers to ensure high-quality governance and timel...Read More>>.

Go back University College London Hospitals NHS Foundation Trust Clinical Research Midwife The closing date is 04 October 2026 We are seeking a highly motivated and passionate Midwife with an interest in clinical rese...Read More>>.

Research NurseLocation: York. 24 hours per week. 6-month contract (potential to be extended). Start: July 2026.What you’ll be doingPerform a variety of complex clinical procedures on subjects including but not limit...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>>.

Have you built your career inhospitality, retail, customer service, leisure, or apeople focusedroleand are now looking for something more structured, rewarding, and with real career progression? As aClinical Research Technician...Read More>>.

This post presents an excellent opportunity to join the establishing and expanding Breast Research team with a varied portfolio of early and late clinical trials as a Clinical Research Nurse (CRN).Research nursing is an exciting and developin...Read More>>.

We can provide emotional and wellbeing support for anyone affected by the Lampard Inquiry. Find support Please be aware that, due to current allocation constraints, Certificates of Sponsorship (CoS) are being prioritised for registered...Read More>>.

Position OverviewResearch Nurse Location: Middlesborough 24 hours per week | 6 months contract (potential to be extended) | Start: July 2026IQVIA is hiring an experienced Clinical Research Nurse to support a hypertension and cardio...Read More>>.

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