10 of 10 Good Clinical Practice Jobs in the South East

have equivalent experience with knowledge of the governance and legislative framework for conducting clinical research studies, including Good Clinical Practice (GCP) , and The UK Policy Framework for Health and Social Care Research.With excellent IT skills, particularly in the use of Web applications and MS Office applications … distribute formal minutes for regular R&I Governance Group Meetings, or oversee this activity To be responsible for overseeing archiving research studies to GCP standards To oversee general filing of R&I documents General: To prioritise own work ensuring adherence to deadlines while delivering within Departmental and Trust guidelines ...

Analytics & Computational SciencesJob Sub Function: BiostatisticsJob Category:Scientific/TechnologyAll Job Posting Locations:High Wycombe, Buckinghamshire, United KingdomJob Description:As a Principal Portfolio Lead, Clinical Programming, this position is responsible for formulating the clinical programming strategy across a set of clinical trial and/or report activities … Skills: Preferred Skills:Advanced Analytics, Biostatistics, Clinical Data Management, Collaborating, Compliance Management, Critical Thinking, Data Privacy Standards, Good Clinical Practice (GCP), Organizing, Presentation Design, Program Management, Quality Assurance (QA), Regulatory Affairs Management, Research Documents, Standard Operating Procedure (SOP), Statistical Analysis Systems (SAS) Programming, Survey DesignSummaryLocation: High ...

description of the role. Main duties of the job We are seeking an experienced HCPC-registered professional to join the Southampton Research and Clinical Histopathology (SRCH) team as a Senior Research and Service Development Lead. This exciting role will lead and coordinate research, service development, innovation and digital pathology … deliver high-quality services and research programmes. The post will support the Trust's strategic objectives by improving patient access to research and clinical trials, driving service improvement, and helping implement innovative technologies that enhance patient care and operational efficiency. Reporting to the Cellular Pathology Research and Service Development ...

## Data Team LeadApplylocations: Reading, Berkshire, United Kingdom: Dublin, Irelandtime type: Full timeposted on: Posted Todayjob requisition id: R1560910**IQVIA is growing! Hiring multiple Clinical Data Management (CDM) Leads across our FSP (Functional Service Provider) and Traditional (Sponsor-Agnostic) delivery models.****Apply now and have your resume considered … Manager*.* Proven success managing large global studies (1000+ patients).* Expertise with Medidata Rave, Oracle InForm, or similar EDC systems.* Strong understanding of GCP, ICH, and clinical research processes.* Excellent communication and leadership skills.**What IQVIA Offers*** Fully remote role – company equipment provided* Competitive salary and performance-based ...

biotechnology and/or pharmaceutical industry, including senior Quality leadership roles in regulated manufacturing environments. Strong knowledge of global regulatory authorities including FDA, GMP, GCP and GLP requirements. Proven expertise in Quality Management Systems (QMS), with a particular focus on GMP compliance and data integrity. Demonstrated experience with regulatory inspections ...

experience in the pharmaceutical industry related to support of clinical systems.Previous Veeva Platform Knowledge preferredGeneral knowledge of and experience working in a GCP environment.Demonstrate communication and technical writing skills.Strong computer and analytical thinking skills.Goal oriented, self-starter with proven ability to work independently.Ability to manage multiple tasks simultaneously … meet deliverables in accordance with stated timelines.Skills RequiredGeneral knowledge of and experience working in a GCP environmentDemonstrated communication, influencing, collaboration and technical writing skillsStrong interpersonal skills and knowledge depth of subject matter to converse with vendors and internal functionsDemonstrated problem solving and strategic thinking skillsGoal oriented, self-starter with proven ...

execution of programs in statistical programming languages within project. Develop complex analysis datasets, specifications, and summary output (tables, listings, or graphs) for inclusion in clinical reports or presentations. Create complex programs that meet regulatory and company standards to permit efficient programming, reporting, and review, utilizing statistical programming languages (e.g … relationship skills including consultative and relationship management skills. Full understanding and knowledge relevant to statistical programming. Full understanding and knowledge of regulatory guidelines (e.g., GCP, ICH, FDA, ISO) relevant to in Pharmaceutical/Medical Device setting. Strong problem-solving, organizational, analytical and critical thinking skills. Experience working in clinical ...

Associate Director Clinical Trial Disclosure and Transparency is a global subject matter expert responsible for ensuring timely, accurate, and compliant clinical trial disclosures across all regions and study types (interventional and observational). This role guides global strategy, drives process excellence, and oversees the delivery of clinical … discussions Strong critical thinking skills, with the ability to make decisions and recommendations in ambiguous situations, escalating appropriately when required. Strong understanding of ICH-GCP, ICMJE, GDPR and industry best practices Demonstrated experience providing strategic oversight of vendors, critically reviewing recommendations and maintaining accountability for final decisions Hands on experience ...

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 architecture … platforms (VENUS, BiOS)Experience with automation scheduling software (Momentum, Cellario, etc.)Familiarity with web services (REST/SOAP) and distributed systemsExperience in regulated environments (GCP, GLP, ISO standards)Knowledge of version control (Git) and Agile methodologiesStrong troubleshooting and communication skillsPay & BenefitsAt Moderna, we believe that when you feel your best ...

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 ...