16 of 16 Good Clinical Practice Jobs in the Thames Valley

trial doses for patients to several departments across the Trust and maintaining up to date documentation according to Good Clinical Practice (GCP). Under the direction of the Accountable Pharmacist and Aseptic Services Manager or Deputy the post holder will be responsible for the provision … support the needs of patients and which meet standards of Good Manufacturing Practice (GMP) and Good Clinical Practice (GCP) This role will involve regular weekend working to support the requirement for Clinical Trial doses at the weekend. About us Oxford University Hospitals NHS Foundation ...

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 ...

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 ...

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 ...

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 ...

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 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 Savvy At Johnson & Johnson,we believe health is everything. Our strength in healthcare ...

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 ...

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 ...

OverviewThe Associate Director, Biostatistics is responsible for statistical activities in support of clinical trials, including contributing to trial designs, authoring statistical sections of protocols, preparing statistical analysis plans, and reviewing and interpreting the analysis of clinical trial data.This is a hybrid position, based two days a week onsite … including RNAi.Desired Experience:· Experience in clinical development through Phase 3 (NDA submission).· Experience as lead statistician for a compound· Understanding of ICH GCP as well as general knowledge of industry practices and standards.· Proficiency in R programming language and other statistical software, including EAST.· Experience with CDISC, including ...

than 60 years developing innovative respiratory diagnostic solutions that help healthcare professionals detect, diagnose and manage respiratory conditions. We are now recruiting for a Clinical Equipment Support Technician to join our team. This is an exciting opportunity to become part of an established global healthcare organisation, working hands … within the Warehouse. Competence in Vitalograph procedures and the Quality Management System (QMS). An understanding of ISO 13485, the Medical Devices Directive and GCP, as required. If youre looking for a hands-on role where you can develop your technical and healthcare knowledge, work alongside experienced teams and build ...

build a career that makes a real difference for patients. At Harwell, you will help shape the future of laboratory automation within Moderna’s Clinical Biomarker Laboratory, driving the development of highly integrated, scalable, and digitally connected laboratory systems. Working at the intersection of automation engineering, biomarker science, data … VENUS, BiOS) Experience with automation scheduling software (Momentum, Cellario, etc.) Familiarity with web services (REST/SOAP) and distributed systems Experience in regulated environments (GCP, GLP, ISO standards) Knowledge of version control (Git) and Agile methodologies Strong troubleshooting and communication skills Pay & Benefits At Moderna, we believe that when ...

Data Acquisition Specialist performs activities relating to the definition, set-up and ingestion of External Data Streams, and related documents and processes aligned with Clinical Trial Protocol defined requirements for data capture.External data streams include but are not limited to typical and novel data collected through central labs … clinical trials. Experience working in highly diverse teams within clinical research; cross-functional, global, multiregional. Knowledge of SDTM. Working knowledge of GCP/ICH guidelines Excellent written and verbal communication in English. This role is not eligible for UK visa sponsorshipIQVIA is a leading global provider of clinical ...

Data Acquisition Specialist performs activities relating to the definition, set-up and ingestion of External Data Streams, and related documents and processes aligned with Clinical Trial Protocol defined requirements for data capture. External data streams include but are not limited to typical and novel data collected through central labs … clinical trials. Experience working in highly diverse teams within clinical research; cross-functional, global, multiregional. Knowledge of SDTM. Working knowledge of GCP/ICH guidelines Excellent written and verbal communication in English. This role is not eligible for UK visa sponsorshipIQVIA is a leading global provider of clinical ...

Vifor in the United Kingdom is seeking a seasoned GCP Auditor to execute the global audit plan, conduct audits of investigator sites, CROs, and IRBs/ECs, and ensure trial data integrity while maintaining compliance with global regulations and company standards. You will report findings, categorize risk levels, and develop … CAPAs, collaborating with multinational teams to implement corrective actions and drive continuous improvement across clinical development; travel up to 50%. #J-18808-Ljbffr ...

oversee programming activities across one or more clinical projects. You will guide a team of programmers, ensure on-time delivery and compliance with GCP and SOPs, and contribute to study design and data analysis strategies. The role emphasizes advanced analytics, collaboration with cross-functional teams, and delivering high-quality ...

statistical programs for clinical data, supporting analysis and reporting with high quality deliverables. You will collaborate with cross-functional teams, ensure compliance with GCP and internal processes, and help drive efficiency through robust programming practices and documentation. #J-18808-Ljbffr ...