1 to 25 of 52 Permanent Good Clinical Practice Jobs in the UK

work within their scope of competence and under the supervision of the Research Lead/team, adhering to Good Clinical Practice (GCP) and relevant research governance frameworks. Main duties of the job The Research Co-ordinator will support the delivery and coordination of research projects, combining clinical … with research teams, sponsors and external partners. All duties will be carried out in accordance with study protocols, Good Clinical Practice (GCP), infection prevention and control standards, GDPR and relevant research governance requirements. About us Medicus Health Partners is the largest GP Partnership in Enfield, caring ...

Trust and KCL requirements. Adhere to the relevant Trust and KCL policies and procedures at all times Report any adverse events as per GCP and the Trust policies. Research Delivery Provide support in research projects as outlined by supervisors. Collaborate with research teams to ensure adherence to trial protocols … Adhere to appropriate policies and legislation regarding clinical research e.g. informed consent, International Conference on Harmonisation (ICH) Good Clinical Practice (GCP). Take responsibility for accurate and complete data collection, updating and maintenance of databases and computerised systems, ensuring corresponding documentation is recorded in medical notes ...

management plans, data dictionaries, CRF completion guidance, study-specific procedures, templates and other supporting documentation. Coordinate the timely collection, electronic entry and verification of clinical data from participating sites, including data required for regulated post-marketing surveillance studies. Review submitted data for completeness, consistency and accuracy, raising and resolving … Degree in life sciences health sciences data management or a related subject or equivalent relevant professional experience Current Good Clinical Practice GCP training Desirable Relevant postgraduate qualification or formal training in clinical research or data management Physical and other requirements Essential Able and willing to travel ...

Quality: You will apply a sound working knowledge of UK research governance, HRA and Research Ethics Committee requirements, Good Clinical Practice (GCP) and sponsor responsibilities. You will ensure appropriate compliance with UK GDPR, the Data Protection Act 2018 and NHS information-governance requirements, maintaining confidentiality and appropriate … degree in life sciences, health sciences, data management or a related subject, or equivalent relevant professional experience. Current Good Clinical Practice (GCP) training. Substantial experience in clinical research, clinical data management or study coordination. Experience designing and implementing paper or electronic Case Report Forms (CRFs ...

ordinators. Adhere to International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) Guideline for Good Clinical Practice (GCP), legislation and policy relating to the conduct of research and according to the study protocol. Assist in the care and follow up of clinical … willingness to undertake Evidence of on-going professional development Desirable International Conference on Harmonisation/Good Clinical Practice (ICH/GCP) certification Experience Essential Interest in mental health care and mental health research. Relevant clinical experience in a patient-facing healthcare clinical role. Experience ...

monitoring and auditing. Maintain awareness of regulatory requirements, i.e. NHS Research Ethics Committee, UK Policy Framework for Health and Social Care Research (2017), ICH-GCP, GDPR, and advise others accordingly. About us The Adam Practice is a partnership located across 5 surgeries in Poole, Dorset. This is an exciting … account of regulations and external requirements e.g. Investigators Site Files (ISFs) Promote and advise on the principles of Good Clinical Practice (GCP) and Good Research Practice within The Adam Practice Research team & DPCCRG. Build and maintain a productive working relationship with colleagues across ...

summary The PCN QOF, Research & Care Coordination Data Analyst is a non-clinical role that combines data analysis, quality improvement, research support, population health management and care coordination within Wellington Medical Centre and Taunton Deane West Primary Care Network (PCN). The role supports the practice in improving … patient outcomes through the effective use of clinical data, identifying patients who may benefit from proactive interventions, and contributing to high-quality, patient-centred care. Wellington Medical Centre is part of Taunton Deane West PCN, which brings together GPs, nurses, pharmacists, social prescribing link workers, health and wellbeing coaches ...

opportunity to buy more, great pension schemes and a number of health and wellbeing initiatives to support you.Closing Date: 13 September 2026The RoleNewcastle Clinical Trials Unit (NCTU) is a thriving UKCRC Registered academic unit, working in collaboration with investigators to design and deliver clinical trials that answer important … clinical questions and bring meaningful impact to patients and the NHS. We are delighted to offer an exceptional opportunity for a Senior Information Systems and Data Manager to join our senior team and lead the strategic development of data management and information systems across the Unit.In this pivotal leadership ...

managing technology solutions that support Research & Early Development activities, particularly within Good Laboratory Practice (GLP) and Good Clinical Practice (GCP) environments. Your expertise will ensure that lab automation platforms and scientific IT systems are effectively integrated, compliant, and aligned with business needs.Who You’ll Work … automation and data managementOversee compliance of GxP IT systems, ensuring proper documentation and validationAct as the DT System Owner (DTSO) for key GLP and GCP applicationsYour focus will be mainly on GCP systems for research, typically systems used for modelling and simulations applications in the Quantitative Clinical Pharmarcology ...

work experience.GPh.C. registered Pharmacy TechnicianDesirableEducational SupervisorLeadership qualification, Management certificate or proven relevant experienceAccredited checking technician (ACPT) Experience/Knowledge EssentialGood Clinical Practice (GCP)Dispensing and Distribution stock control systemsProven experience in training and assessment of junior staffRelevant Hospital pharmacy experience as a qualified Technician.Operation of Automated Dispensing Robot … work experience.GPh.C. registered Pharmacy TechnicianDesirableEducational SupervisorLeadership qualification, Management certificate or proven relevant experienceAccredited checking technician (ACPT) Experience/Knowledge EssentialGood Clinical Practice (GCP)Dispensing and Distribution stock control systemsProven experience in training and assessment of junior staffRelevant Hospital pharmacy experience as a qualified Technician.Operation of Automated Dispensing Robot ...

France, Italy, Czech Republic, Bulgaria.Job Description SummaryThis unique role within IQVIA is ideal for someone with a technical mindset, strong communication skills, and a good understanding of SDTM.Experience in Study Design, CRF annotation, CDISC standards, and vendor management will be key for success in this position. The role … into standard and SDTM.• In collaboration with Study Data Leads ensure the planning for data receipt and its oversight throughout the duration of assigned clinical trials• Program reports and contribute to the standardization of process and reports used for data review and analysis for external partners/vendors ...

problem-solving skillsHigh levels of initiative, drive and commitment. Prior experience in a Data Management related field is requiredExperience with relational databases, preferably Clinical Data Management and EDC SystemsExperience communicating with all levels of personnel and participating in collaborative work team (locally and globally).Advanced knowledge of federal regulations … Good Clinical Practice, and Good Clinical Data Management Practices.Excellent command, both verbal and written, of EnglishThis role is not eligible for UK visa sponsorshipIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare ...

problem-solving skillsHigh levels of initiative, drive and commitment. Prior experience in a Data Management related field is requiredExperience with relational databases, preferably Clinical Data Management and EDC SystemsExperience communicating with all levels of personnel and participating in collaborative work team (locally and globally).Advanced knowledge of federal regulations … Good Clinical Practice, and Good Clinical Data Management Practices.Excellent command, both verbal and written, of EnglishThis role is not eligible for UK visa sponsorshipIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare ...

Function: Data Analytics & Computational SciencesJob Sub Function: BiostatisticsJob Category:Scientific/TechnologyAll Job Posting Locations:High Wycombe, Buckinghamshire, United KingdomJob Description:Position SummaryThe Experienced Clinical Programmer is an experienced clinical trial programmer with in-depth knowledge in industry standard and complex data structures, programming languages, and/… Reasoning, Biological Sciences, Biostatistics, Clinical Trials, Data Modeling, Data Privacy Standards, Data Quality, Data Savvy, Detail-Oriented, Good Clinical Practice (GCP), Report Writing, Research Ethics, Researching, Statistical Analysis Systems (SAS) Programming, Statistics, Technologically SavvySummaryLocation: High Wycombe, Buckinghamshire, United KingdomType: Full time ...

looking for a Public Health Research Analyst to support quantitative research and evaluation across Public Health Wales, contributing to work that informs policy, practice and better outcomes for people and communities across Wales. You will work with routine, survey and linked datasets to prepare, clean, manage, analyse and interpret … software such as R, Python, SQL, or Excel, depending on the project and your existing skills. Follow information governance, data protection, confidentiality, accessibility and good research-practice requirements. Manage your workload across projects, contribute to teamplanning and raise risks or data-quality issues promptly. About ...

accordance to departmental processes and procedures. This position is accountable for the planning, oversight and delivery of statistical programming activities supporting one or more clinical projects, compounds and/or submissions generally of low-medium complexity/criticality. The Senior Statistical Programming Lead is responsible for making decisions … Analytics, Biostatistics, Clinical Trials, Collaboration, Consulting, Critical Thinking, Data Privacy Standards, Data Quality, Data Savvy, Digital Fluency, Good Clinical Practice (GCP), Quality Assurance (QA), Report Writing, Standard Operating Procedure (SOP), Statistical Analysis Systems (SAS) Programming, Statistics, Systems Development, Technologically SavvySummaryLocation: High Wycombe, Buckinghamshire, United KingdomType: Full ...

accordance to departmental processes and procedures. This position is accountable for the planning, oversight and delivery of statistical programming activities supporting one or more clinical projects, compounds and/or submissions generally of low-medium complexity/criticality. The Senior Statistical Programming Lead is responsible for making decisions … Analytics, Biostatistics, Clinical Trials, Collaboration, Consulting, Critical Thinking, Data Privacy Standards, Data Quality, Data Savvy, Digital Fluency, Good Clinical Practice (GCP), Quality Assurance (QA), Report Writing, Standard Operating Procedure (SOP), Statistical Analysis Systems (SAS) Programming, Statistics, Systems Development, Technologically Savvy #J-18808-Ljbffr ...

with departmental processes and procedures. This position is accountable for the development, verification, and documentation of code used for the analysis and reporting of clinical data and is responsible for the timeliness and the quality of assigned deliverables supporting clinical projects and submissions. This position is a member … Reasoning, Biological Sciences, Biostatistics, Clinical Trials, Data Modeling, Data Privacy Standards, Data Quality, Data Savvy, Detail-Oriented, Good Clinical Practice (GCP), Report Writing, Research Ethics, Researching, Statistical Analysis Systems (SAS) Programming, Statistics, Technologically SavvySummaryLocation: High Wycombe, Buckinghamshire, United KingdomType: Full time ...

dispensing systems, and the Aerocom pneumatic tube system, ensuring seamless medication storage, dispensing, and distribution across the hospital. Working closely with Pharmacy, IT, and clinical teams, you will support system improvements, training, troubleshooting, and compliance with regulatory standards to enhance patient safety and operational efficiency. The role involves investigating … Educational Supervisor Leadership qualification, Management certificate or proven relevant experience Accredited checking technician (ACPT) Experience/Knowledge Essential Good Clinical Practice (GCP) Dispensing and Distribution stock control systems Proven experience in training and assessment of junior staff Relevant Hospital pharmacy experience as a qualified Technician. Operation ...

Computer System Validation & GCP Compliance Consultant Company: Pharmaceutical/Biotech Quality and Regulatory Consultancy Location: Remote (UK) - Multiple Positions Package: Excellent hourly rates offered in line with experience, with the potential of a salaried position in the future. The Role in 20 Seconds You’ve spent several years working … validation specialist, a quality lead, or the person a clinical operations team calls when a system needs to be inspection-ready. You know GCP well enough to spot the difference between a genuine data integrity risk and a paperwork exercise. You know how to walk into a clinical ...

with academic, NHS and industry partners. We are looking for someone with substantial experience of research management, trial management or operational delivery in a clinical, scientific or academic environment, including portfolio, budget and reporting responsibilities. Experience of line management and multidisciplinary working, together with knowledge of clinical research … Manager will support the Directors in the operational management and coordination of the Radiology Research Group and Artificial Intelligence Imaging Hub, working across scientific, clinical and research support teams. The post holder will coordinate the people, processes and partnerships needed to deliver agreed imaging and AI research priorities ...

CoMind, we are developing a non-invasive neuromonitoring technology that will result in a new era of clinical brain monitoring. In joining us, you will be helping to create cutting-edge technologies that will improve how we diagnose and treat brain disorders, ultimately improving and saving the lives … Senior Optical Research Scientist at CoMind, you will join a highly interdisciplinary team working at the interface of optics, engineering, neuroscience, data science, and clinical neuromonitoring. This is a hands‐on senior scientific role. You will design, run, troubleshoot, and analyse experiments using prototype and production‐ready optical systems ...

Senior Clinical Data … Coordinator performs activities pertaining to the conduct of Phase I-IlI clinical trials in accordance with ICH/Good Clinical Practices (GCP) and other relevant procedures and guidelines to ensure that a quality work product is produced and timelines and deliverables are met.Summary of the Essential Functions ...

Senior Clinical Data … Coordinator performs activities pertaining to the conduct of Phase I-IlI clinical trials in accordance with ICH/Good Clinical Practices (GCP) and other relevant procedures and guidelines to ensure that a quality work product is produced and timelines and deliverables are met.Summary of the Essential Functions ...

Senior Clinical Data … Coordinator performs activities pertaining to the conduct of Phase I-IlI clinical trials in accordance with ICH/Good Clinical Practices (GCP) and other relevant procedures and guidelines to ensure that a quality work product is produced and timelines and deliverables are met.Summary of the Essential Functions ...