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>>.

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: Clinical Research NurseBanding: Band 5/6Location: NottinghamHourly Pay Rate: £25 - £30 per hour What You'll Do Carry out participant visits, observations, interventions and safety checks in line...Read More>>.

Job Title: Clinical Research NurseBanding: Band 5/6Location: MiddlesbroughHourly Pay Rate: £25 – £30 per hour Join a team driven by one purpose — improving global health outcomes. Our client is looking for a dedicate...Read More>>.

Tigermed is seeking an experienced Clinical Research Associate in Manchester to oversee site management, training, and documentation across trials in line with ICH-GCP and sponsor requirements. You will ensure site initiation, monitoring visits, s...Read More>>.

Queen’s University Belfast seeks an exceptional Head of Operations to build and lead the NICRF within iREACH Health, driving operational excellence and research delivery across academic, NHS and industry partnerships.Reporting to the NICR...Read More>>.

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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>>.

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Pulse Healthcare in Manchester is seeking a dedicated Clinical Research Physician to join our team in the North West. The role involves conducting clinical trials, ensuring regulatory compliance, and advancing medical knowledge.Flexible, of...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>>.

Celerion is seeking a full-time Biostatistician for our Data Management and Biometric department in the United Kingdom. You will develop statistical analysis plans, perform SAS-based analyses, and prepare reports for assigned projects, contributin...Read More>>.

Reporting to: Professor Nick James and Dr Hoda Abdel-Aty Duration ofContract: Fixed Term for 24 months in the first instance Hours per week : 40 hours per week (Full Time). Less than Full time (LTFT) may b...Read More>>.

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Junior User Researcher - Associate Consultant - Digital Excellence - LondonReference Code: 350231-en_GBContract Type:PermanentProfessional Communities: Strategy & Transformation....Read More>>.

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