17 of 17 Remote/Hybrid Good Clinical Practice Jobs in England

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 ...

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 ...

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 ...

drug development. As Associate Director Statistical Programming, you will lead a high-performing community of programmers, driving innovation, quality, and efficiency across complex clinical programs. You’ll play a critical role in delivering timely, high-quality insights that enable life-changing treatments to reach patients faster—while empowering teams … relevant degree.Proven leadership, collaboration and organizational skills with demonstrated ability to successfully manage simultaneous trials and meet deadlinesExcellent understanding of clinical trials methodology, GCP and medical terminologyMust be able to anticipate challenges and risks and proactively suggest/implement solutionsAbility to work under pressure demonstrating agility through effective ...

PRINCE II certification is a plusIn-depth project management experience ideally within clinical researchExperience and understanding of the clinical research environment and GCP principlesStrong leadership, diplomatic and motivational skillsOpen, transparent and excellent communication skills, fluency in English both verbal and writtenProven ability to work creatively and analytically … large and diversified audience. Ability to adjust presentation material for differing audienceSolid technical background, with understanding or hands-on experience in software development and clinical technologies (EDC, eCOA, IWRS etc.)Strong working knowledge of Microsoft Office toolsThis role is not eligible for UK visa sponsorship.IQVIA is a leading global ...

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 ...

Please only apply if this location is accessible for you. Therapy Area - NeuroscienceStep into a pivotal role where your expertise shapes the future of clinical development. As a Senior Principal Statistical Programmer, you will lead complex programming strategies across high-impact studies and programs, partnering with cross-functional teams … structures as well as a solid understanding of the development and use of standard programsGood understanding of regulatory requirements relevant to Statistical Programming (e.g. GCP, study procedures)Proven communications and negotiation skills, ability to work well with others globally and influenceExperience as Trial/Lead/Program Programmer for several ...

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 ...

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 ...

Standout is seeking a Computer System Validation & GCP Compliance Consultant to work remotely in the UK. You’ll lead validation projects for clinical trial systems such as EDC, IRT, CTMS, eTMF and ePRO, and you’ll conduct GCP audits with practical, risk‐based approaches. The role focuses on senior ...

Novartis is seeking a Monitoring - Functional Excellence Lead to drive data-driven monitoring across clinical trials from London (The Westworks) or remote … UK. This role shapes adaptive monitoring strategies, delivering operational impact at scale and enhancing trial quality, efficiency and patient outcomes. As part of the GCP Excellence Monitoring team, you will champion innovative approaches, influence monitoring implementation globally, and partner with cross-functional teams to #J-18808-Ljbffr ...