8 of 8 Remote GxP Jobs in the UK

exposure to clinical trials. Clinical, pharmacological, and therapeutic knowledge in neuroscience. Good understanding of clinical study design principles and basic familiarity working with clinical data in a clinical trial (GxP) setting. Strong knowledge and understanding of (multivariate implementations of) statistical methods such as time to event analysis, machine learning, meta-analysis, mixed effect modelling, longitudinal modelling, Bayesian methods, variable selection More ❯

technical teams. Structured, proactive, and able to work independently as the "go-to" person for data. Industry Requirement Pharmaceutical industry experience is mandatory. Experience working in a regulated environment (GxP, CSV compliance) preferred. What We Offer Fully remote engagement (global team). Long-term contract with high client visibility. Opportunity to lead significant data workstreams in a major pharma program. More ❯

year undergraduate degree 10+ years' experience in a Regulatory Affairs role in the pharmaceutical industry, experience with Health Canada, EMA, MHRA and other local European agencies preferred Understanding of GxP systems and Quality principles Ability to research global regulatory guidance (nonclinical, clinical and CMC) and precedence to assist in the development and execution of global regulatory strategies. Knowledge of eCTD More ❯

a strong emphasis on stakeholder management and effective communication with senior managers and directors. What are we looking for? Experience delivering business changes or IT business system projects to GxP environment, either in a pharma site or equivalent a must have Demonstrated experience in IT Project Management. Demonstrated experience in stakeholder management and presenting to senior managers and directors. Experience More ❯

Head of Software Development Basic Salary – £70-80k (Neg) with bonus and package Home based role with access to prestigious offices in the Manchester area circa 1-2 times per week Solution — The “data” held within Electronic Health records More ❯

partners to ensure seamless solution delivery, system integration, and regulatory compliance. You’ll play a key part in bridging the gap between business needs and technical execution within a GxP-regulated environment. Key Responsibilities: Collaborate with site quality teams to gather and analyse business requirements. Configure and deploy Biovia OneLab workflows, protocols, and templates aligned with operational needs. Work with … successful solution delivery and alignment with Biovia platform capabilities . Set up and manage integrations with enterprise systems such as LIMS, ELN, ERP, and MES . Ensure compliance with GxP , 21 CFR Part 11 , and internal validation protocols. Troubleshoot and resolve configuration and integration issues. Document configuration and integration processes for validation and audit readiness . Provide training and user … Biovia OneLab configuration and deployment Strong knowledge of system integration , including APIs, middleware, and data exchange protocols Deep understanding of Quality Management Systems (QMS) and laboratory workflows Familiarity with GxP compliance , validation documentation , and audit processes Excellent problem-solving, communication, and documentation skills If you are interested or would like to know more, please email jonathan.la@focusonsap.org with your CV More ❯

partners to ensure seamless solution delivery, system integration, and regulatory compliance. You’ll play a key part in bridging the gap between business needs and technical execution within a GxP-regulated environment. Key Responsibilities: Collaborate with site quality teams to gather and analyse business requirements. Configure and deploy Biovia OneLab workflows, protocols, and templates aligned with operational needs. Work with … successful solution delivery and alignment with Biovia platform capabilities . Set up and manage integrations with enterprise systems such as LIMS, ELN, ERP, and MES . Ensure compliance with GxP , 21 CFR Part 11 , and internal validation protocols. Troubleshoot and resolve configuration and integration issues. Document configuration and integration processes for validation and audit readiness . Provide training and user … Biovia OneLab configuration and deployment Strong knowledge of system integration , including APIs, middleware, and data exchange protocols Deep understanding of Quality Management Systems (QMS) and laboratory workflows Familiarity with GxP compliance , validation documentation , and audit processes Excellent problem-solving, communication, and documentation skills If you are interested or would like to know more, please email jonathan.la@focusonsap.org with your CV More ❯

partners to ensure seamless solution delivery, system integration, and regulatory compliance. You’ll play a key part in bridging the gap between business needs and technical execution within a GxP-regulated environment. Key Responsibilities: Collaborate with site quality teams to gather and analyse business requirements. Configure and deploy Biovia OneLab workflows, protocols, and templates aligned with operational needs. Work with … successful solution delivery and alignment with Biovia platform capabilities . Set up and manage integrations with enterprise systems such as LIMS, ELN, ERP, and MES . Ensure compliance with GxP , 21 CFR Part 11 , and internal validation protocols. Troubleshoot and resolve configuration and integration issues. Document configuration and integration processes for validation and audit readiness . Provide training and user … Biovia OneLab configuration and deployment Strong knowledge of system integration , including APIs, middleware, and data exchange protocols Deep understanding of Quality Management Systems (QMS) and laboratory workflows Familiarity with GxP compliance , validation documentation , and audit processes Excellent problem-solving, communication, and documentation skills If you are interested or would like to know more, please email jonathan.la@focusonsap.org with your CV More ❯