13 of 13 Permanent Good Clinical Practice Jobs in the UK excluding London

patients throughout their research journey, collect clinical data and ensure studies are delivered safely in line with Good Clinical Practice (GCP) and regulatory requirements. You will join a forward-thinking practice that values innovation, teamwork and continuous improvement, with opportunities to develop your research skills … support participants throughout their research journey, ensuring safe, compassionate and effective care in line with approved study protocols, Good Clinical Practice (GCP), research governance requirements and practice procedures. The role will involve identifying and recruiting eligible participants, conducting study visits, supporting clinical assessments, collecting samples ...

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 ...

with children and young people will involve supporting, coordinating, and overseeing research studies in line with the competencies of the role and scope of practice under the NMC registration. This includes ensuring adherence to ethical, legal and regulation standards. Maintaining accurate records and ensuring patient safety, paying great attention … other specialities Previous experience in an acute Trust Awareness of relevant legal and regulatory framework governing clinical practice Desirable Research training (e.g. GCP, degree module, informed consent) Teaching qualification Additional certificate or courses related to RCHT Aditional circumstances Essential Able to travel across sites and to attend external ...

administrative service for the Radiopharmacy Department and the Head of Department. Maintain manufacturing study files and documentation oversee and follow up on Trust-wide GCP training, and manage the DocuSign Radiopharmacy contracts signature process. This includes data collection and entry for suppliers and customers, maintaining databases, spreadsheets, and logs … facilitating Trust-wide communication to ensure GCP training compliance for all Radiopharmacy research staff in accordance with Trust requirements. About us Our Trust Cambridge University Hospitals (CUH) NHS Foundation Trust comprises Addenbrooke's Hospital and the Rosie Hospital in Cambridge. With over 13,000 staff and over 1100 beds ...

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 ...

Technical/Cancer Services Pharmacist, you will play a key role in delivering and developing high-quality technical and cancer services. You will support clinical screening, act as a Releasing Officer for pharmaceutical products compounded under the Manufacturer's Specials Licence, and contribute to the Pharmaceutical Quality System … ensure product quality, regulatory compliance and patient safety. Working closely with multidisciplinary teams, you will provide expert clinical and technical advice, lead service development and quality improvement initiatives, contribute to governance activities, and help ensure the safe, effective and efficient use of medicines across Cancer Services. This ...

quality processes and systems, implementing best-in-class frameworks to enhance efficiency, compliance, and scalability. Ensure all clinical operations adhere to ICH-GCP guidelines (R2/R3), applicable regulations, and internal quality standards. Lead the implementation, improvement and validation of new processes, procedures, and IT systems (e.g., eQMS, eTMF … solutions, and GxP-relevant systems. Embed a culture of quality awareness through training, workshops, and mentoring, ensuring all staff are competent and compliant with GCP, ISO standards, and internal policies. Support the Quality Manager in maintaining the Business Management System (BMS) as it relates to GCP and clinical operations. ...

quality processes and systems, implementing best-in-class frameworks to enhance efficiency, compliance, and scalability. Ensure all clinical operations adhere to ICH-GCP guidelines (R2/R3), applicable regulations, and internal quality standards. Lead the implementation, improvement and validation of new processes, procedures, and IT systems (e.g., eQMS, eTMF … solutions, and GxP-relevant systems. Embed a culture of quality awareness through training, workshops, and mentoring, ensuring all staff are competent and compliant with GCP, ISO standards, and internal policies. Support the Quality Manager in maintaining the Business Management System (BMS) as it relates to GCP and clinical operations. ...

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 ...

## 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 ...

those patients who will benefit most and delivering companion or complementary diagnostic assays aligned to drug development to enable personalised healthcare across our clinical portfolio. We are seeking a Senior Scientist to join our Accredited Diagnostic Development Laboratory (ADDL) at the Cambridge Biomedical Campus, supporting the development, optimisation, validation … remains inspection-ready and trusted. * Clinical Trial Testing Support: Perform and oversee prospective diagnostic testing for clinical studies, ensuring GCP ICH adherence, sample integrity, accurate data capture, and dependable reporting timelines. * Process Engineering and System Integration: Improve end-to-end laboratory workflows by integrating LIMS and related systems ...

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 ...

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 ...