19 of 19 Permanent Good Clinical Practice Jobs in the UK

and Development Grade: NHS AfC: Band 4 Contract: Permanent Hours: Full time - 37.5 hours per week Job ref: 309-UCLH-5888 Site: NIHR UCLH Clinical Research Facility Town: London Salary: £31,944 - £34,937 Per annum inclusive of HCAS Salary period: Yearly Closing: 20/02/:59 The … studies. The post holder will ensure high quality data in line with the study protocol, the principles of Good Clinical Practice (GCP) and the UK Medicines for Human Use (Clinical Trials) Regulations. The post holder will be based across both CRF sites according to the needs … equivalent, with Grade C or above in English and Maths. Knowledge of drug development process and concept of clinical trials Knowledge of ICH GCP Science related degree or equivalent Experience Experience of dealing with confidential information Experience of working with clinical trials Skills & Abilities Ability to make decisions More ❯

Medical Writing, to drive efficiency and accountability. IQVIA Biostatistics helps interpret and draw inferences from data collected on patients as they progress through a clinical trial and serves as the bridge between data capture and reporting. We have one of the largest Biostatistics departments within the industry of around … needs analysis for complex project or client requirements. Acting as a lead on studies, you will directly communicate with internal and client statisticians and clinical team members to ensure appropriate understanding of requirements and project timelines and support the training of new or junior team members. As well as … and coordinating tasks within a programming team In-depth knowledge of applicable clinical research regulatory requirements, i.e. Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Join IQVIA to see where your skills can take you Global exposure Variety of therapeutic areas Collaborative and More ❯

Medical Writing, to drive efficiency and accountability. IQVIA Biostatistics helps interpret and draw inferences from data collected on patients as they progress through a clinical trial and serves as the bridge between data capture and reporting. We have one of the largest Biostatistics departments within the industry of around … needs analysis for complex project or client requirements. Acting as a lead on studies, you will directly communicate with internal and client statisticians and clinical team members to ensure appropriate understanding of requirements and project timelines and support the training of new or junior team members. You will estimate … and coordinating tasks within a programming team In-depth knowledge of applicable clinical research regulatory requirements, i.e. Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Join IQVIA to see where your skills can take you Global exposure Variety of therapeutic areas Collaborative and More ❯

in statistical reporting, along with a proven track record in operational or functional leadership, is required. About the Role Lead SP activities for multiple clinical trials within a program or an indication/disease area. Experience in one of the TA areas: Immunology, Cardiovascular & Metabolic Diseases and Neuroscience is … nurture statistical programmers. Conduct performance appraisal of direct reports, as applicable. Build and maintain effective working relationships with cross-functional team members within the clinical trial/program, and able to summarize and discuss status of deliverables and critical programming aspects with them (timelines, scope, resource plan). Maintain … conferences or consortiums (e.g. CDISC). Experience: In-depth understanding of clinical trials methodology, regulatory requirements, and Good Clinical Practice (GCP). Demonstrated leadership, collaboration, and organizational skills with the ability to successfully manage and oversee multiple trials simultaneously, ensuring deadlines are met. BS/MS More ❯

at Syneos Health Project Data Manager Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Description Project Data Manager Syneos Health is a leading fully integrated biopharmaceutical … solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to … belong. Job Responsibilities Acts as Functional Lead for Data Management including primary contact for internal liaison between Data Management/Operations and Project Management, Clinical Monitoring, and other functional groups Coordinate the work of the assigned Data Management/Data Operations team Ensures launch, delivery and completion of all More ❯

some of our hospitals are provided by our PFI partners. For these jobs, please seevacancies with our PFI partners . Aseptic Services Manager for Clinical Trials Aseptic Services Unit NHS AfC: Band 7 Main area Pharmacy Aseptic Services Grade NHS AfC: Band 7 Contract Permanent Hours Full time - 37.5 … for Human Use (Clinical Trials) Regulation (EU Directive 2001/20EC), Human Medicines (EU Exit) Regulations 2019 and the International Conference on Harmonisation GCP Guideline (ICH GCP), as applicable to the dispensing of Investigational Medicinal Products for clinical trials or other products. To ensure the preventative maintenance and … for Human Use (Clinical Trials) Regulation (EU Directive 2001/20EC), Human Medicines (EU Exit) Regulations 2019 and the International Conference on Harmonisation GCP Guideline (ICH GCP), as applicable to the dispensing of Investigational Medicinal Products for clinical trials or other products eg NIMPs, physiological compounds given to More ❯

and best practices related to CSV to improve inhouse CSV process by identifying areas for enhancement and implementing best practices. Must possess understanding of GCP, GLP, and GMP principles and procedures. Must possess excellent verbal and written communication skills. Proficient in MS Word and other Office applications. A strong team More ❯

and best practices related to CSV to improve inhouse CSV process by identifying areas for enhancement and implementing best practices. Must possess understanding of GCP, GLP, and GMP principles and procedures. Must possess excellent verbal and written communication skills. Proficient in MS Word and other Office applications. A strong team More ❯

and best practices related to CSV to improve inhouse CSV process by identifying areas for enhancement and implementing best practices. Must possess understanding of GCP, GLP, and GMP principles and procedures. Must possess excellent verbal and written communication skills. Proficient in MS Word and other Office applications. A strong team More ❯

your dream job, you'll also be helping to save the planet! THE ROLE We are seeking a Senior Programmer to work across multiple clinical and non-clinical studies; supporting regulatory submission activities; producing and validating datasets and outputs to excellent quality whilst adhering to deliverable timelines. Excellent … to company resourcing meeting Point of contact for programming issues for the team, proactively ensuring everything is working cohesively Persuade stakeholders to follow best practice within a trial Develop and deliver company-wide training as and when required Identify areas where new processes are required Create, review and update … the pharmaceutical industry Good awareness of clinical trial issues, design, and implementation Experience of regulatory submissions and associated industry guidance Familiarity with GCP and regulatory requirements Knowledge of SDTM and ADaM CDISC standards APPLY NOW With the world's eyes focused on clinical trial data, this is More ❯

our clients' cutting-edge research, helping innovative biopharmaceuticals, monoclonal antibodies, biomarkers and immuno-oncology treatments gain regulatory approval. We are a niche GLP and GCP compliant laboratory with our experienced scientific team providing specialist immunohistochemistry (IHC), histology, digital pathology and image analysis solutions, working with pharmaceutical and biotechnology companies worldwide. More ❯

our clients' cutting-edge research, helping innovative biopharmaceuticals, monoclonal antibodies, biomarkers and immuno-oncology treatments gain regulatory approval. We are a niche GLP and GCP compliant laboratory with our experienced scientific team providing specialist immunohistochemistry (IHC), histology, digital pathology and image analysis solutions, working with pharmaceutical and biotechnology companies worldwide. More ❯

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to … s degree, in a quantitative or scientific discipline, or local equivalent. A minimum of 5 years relevant experience in SAS programming, preferably in the clinical research industry. Prior relevant experience in SAS programming, preferably in the clinical research industry. Ability to perform assigned tasks under minimal supervision, as … problem solving and organizational skills, attention to detail, verbal a communications skills. Understanding of global clinical trial practices, procedures, methodologies and requirements (e.g., GCP, ICH). Familiarity with the types of risks associated with a study and the impact on key parameters, such as study timelines. Demonstrated ability to More ❯

Product Manager - Health Tech Company Join Us in Revolutionising Healthcare! Are you passionate about leveraging technology for the greater good? Here's your chance to make a tangible impact on global health! This cutting-edge Health Tech Company is at the forefront of innovation. Be part of the journey … experience in healthcare technology Working knowledge of healthcare data standards, particularly FHIR Product analytics, UI/UX feedback loops, and process optimization Experience with clinical workflows and healthcare IT systems Strong analytical and problem-solving skills Excellent communication and stakeholder management abilities Bachelor's degree in a relevant field … based data exchange, data mapping, and validation rules Experience with clinical research or EDC systems Knowledge of regulatory requirements for clinical trials (GCP, 21 CFR Part 11) Familiarity with Agile development methodologies What's On Offer Competitive Salary and Benefits: We value our team and offer a competitive More ❯

regulatory intelligence activities, the SOP and WP management, and the project liaison activities. In close collaboration with the Head of Global Quality Management of GCP, CSV & GVP, Senior Director Global Quality Management and the CSV Audit Lead: QUALIFICATIONS/EXPERIENCE REQUIRED Degree in natural science or equivalent business experience Several … IT) industry/pharmaceutical industry/medical devices industry/Regulatory Authority or otherwise relevant experience, preferably including Quality Assurance for Manufacturing, Pharmacovigilance and Clinical Development and Computerised System Validation and Data Integrity Expert knowledge/experience in relevant regulations and guidance documents, e.g., in the area of Computerised … System Validation, Data Integrity, Manufacturing, Pharmacovigilance, Clinical Development, Medical Device, IMP management, Regulatory Affairs and Pharmacovigilance Experience as a Lead Auditor on internal audits and external vendor audits. Experienced in GxP related CSV audits and inspections Knowledge and understanding of computerised systems in the GxP environment, experience in software More ❯

The R&D Forum will list jobs that are relevant to the sector and are posted by non-commercial organisations. Organisation: Oncology Clinical Trials Office (OCTO), Dept Oncology, Oxford University Type: Full Time Basis of Employment: Contract Description: Senior Data Manager, OCTO Department of Oncology, Oncology Clinical Trials … Department, Churchill Hospital, Headington, Oxford, OX3 7LE About the role We have an exciting opportunity for a Senior Data Manager to join the Oncology Clinical Trials Office (OCTO). OCTO, part of the University of Oxford's Department of Oncology, is a leader in early cancer detection, precision prevention … within clinical trials, including CTIMPs, in a sponsor organisation. You will have experience of implementing approaches to ensure compliance with high standards of GCP, the requirements of UK clinical trials and data protection legislation, and will have experience of developing and delivering training in relation to data management More ❯

in the first instance Hours: Full time About the role We have an exciting opportunity for a Senior Data Manager to join the Oncology Clinical Trials Office (OCTO). OCTO, part of the University of Oxford's Department of Oncology, is a leader in early cancer detection, precision prevention … and therapy trials, delivering groundbreaking clinical research. As the Senior Data Manager, you will be responsible for ensuring that data collection systems and data management activities are appropriately designed, implemented, maintained, or developed to support the collection of high-quality clinical trial data sets for analysis, publication, and … within clinical trials, including CTIMPs, in a sponsor organisation. You will have experience of implementing approaches to ensure compliance with high standards of GCP, the requirements of UK clinical trials and data protection legislation, and will have experience of developing and delivering training in relation to data management More ❯

re establishing new ways to think about science, manufacturing, and commercialization. And new ways to think about health. As a key member of Global Clinical Trial Services team, Regeneron is now looking for a Senior Manager, Digital Health Technologies, who will lead the implementation of digital tools & technologies in … clinical research studies. A great opportunity to join a passionate, dedicated & collaborative international team. Senior Manager, Digital Health Technologies Office Based - Uxbridge What you'll be doing: Implement and coordinate digital tools and technologies (e.g., eCOA, eConsent, wearables, sensors, spirometry, ECG) in individual clinical research studies from study … and written, with the ability to influence and work collaboratively. Technical proficiency in trial management systems and Microsoft Project Server. Knowledge of ICH/GCP and regulatory guidelines/directives. Project management skills, cross-functional team leadership, and organisational abilities. To be considered for this opportunity you must have 8+ More ❯

you'll benefit from a scale of opportunity that is nothing short of extraordinary. We've also created a digitally enabled organisation to improve clinical quality, patient & staff experience, operational effectiveness & driving research, and innovation through the introduction of Hive; our Electronic Patient Record system which launched in September … application, email our team at . We're looking forward to hearing from you! Person specification Qualifications and Training Full GMC Registration. Research qualification Clinical Experience Experienceof working with Burn injured adults and children Registrar level experience in Burn care Knowledge and Skills ability to work as an effective … or equivalent. Ability to teach clinical and operative skills Trainer/coordinator of a recognised course in burns (eg EMSB/ABLS). GCP Certificate GCP Certificate Employer certification/accreditation badges You must have appropriate UK professional registration. This post is subject to the Rehabilitation of Offenders Act More ❯