26 to 36 of 36 Good Clinical Practice Jobs in the UK excluding London

role: Applying innovative statistical approaches to solve novel data challenges Leading projects, ensuring efficient project management, compliance, and high-quality deliverables Analysing phase III clinical trial data in order to support HTA submissions Providing statistical consultancy to internal and external customers Planning, analysing, and visualising observational and real-world … with proven industrial experience Knowledge of HTA-related statistical methods, including ITC, NMA, and complex statistical modelling techniques Awareness of regulatory standards, ICH/GCP guidelines, and HTA regulations Understanding of the clinical drug development process Proficiency in statistical programming languages (SAS and/or R) Strong problem-solving more »

of Quality Assurance is to promote a quality culture of continuous improvement to ensure all systems and procedures undertaken are in compliance with ICH-GCP guidelines and other regulatory requirements. Main Responsibilities Ensure Non-Conformances/Incident Reports are reviewed, assessed and approved using the eQMS ensuring it is contributing … to continual quality improvement. Ensure Quality Documents are reviewed for process improvements, are of a high standard in accordance with ICH-GCP, and approved using the eQMS. Ensure external Sponsor audits or Inspections are prepared, hosted including timely provision of document requests, and for any findings CAPAs are raised, reviewed … necessary. Organising QA training for all staff - including distributing workload and monitoring task completion. Qualifications and Experience: At least 6 years of experience in GCP Quality Assurance within the Pharmaceutical Industry. Strong knowledge of Quality Management Systems within the Pharmaceutical industry. Strong knowledge of ICH-GCP and GMP guidelines. Experience more »

you to have: BSc/MSc/PhD in Chemistry (or related scientific discipline) A sound working knowledge of relevant quality standards; GMP, GLP, GCP and other analytical related quality standards Good working knowledge of Quality Assurance in the Chemical and Pharmaceutical Industry Quality Assurance background which includes some … attention to detail Impressive written and verbal communication ABOUT THE OPPORTUNITY You will provide general support to Quality Assurance activities relating to GLP, GMP, GCP, and other similar Quality Systems established to ensure that the appropriate standards and effective working systems and relationships are maintained and where necessary improved. Responsible … for auditing GLP, GCP and GMP plans, raw data, study procedures and related facilities to ensure compliance with current relevant regulatory requirements and internal consistency, Identify and report any areas of non-compliance to both study and facility management. Liaise with key stakeholders, providing them with accurate information and progress more »

via literature searches. Providing an indication of any potential difficulties with bioanalytical methods and assisting with client calls and visits. Working to GLP/GCP and showing good documentation practice. The Person A successful candidate will have previous experience working in a regulatory bioanalysis lab with experience performing LC … experience of using LC-MS/MS. Previous experience of troubleshooting Have previous experience performing sample extraction techniques for biological analysis. Must be a good communicator with excellent interpersonal skills. Important Information: We endeavour to process your personal data in a fair and transparent manner. In applying for this more »

Assurance department. - Knowledge of GxP and Quality related regulations and standards within the Pharmaceutical/Medical Device industry. - Familiarity with ISO 9001, ISO 13485, GCP is essential. - Knowledge of ISO 21CFR Part 820, ISO17025, Clinical Trials experience, ISO13485 Lead auditor would be beneficial. Interested or know someone who might more »

debilitating disease areas. Our guiding principles, centred around Integrity and Patient-Centricity, are at the heart of everything we do. Job Purpose Lead all Clinical Data Management (CDM) lifecycle activities from protocol inception to database delivery for numerous global studies via oversight of multiple vendors and internal/external … database locks. Participates in Service Provider selection, evaluation and management, including reviewing and providing input to scope of work. Coordinates user acceptance testing for clinical databases. Contributes to global and sub functional working groups and initiatives. Responsibilities Responsible for delivery of clinical global study databases and specific study … is an essential part of the position Working as the sole Data Manager within the Team Key skills and experience In depth knowledge of GCP and current legislation. Working knowledge of Medidata Rave ( desirable but not essential) and IBM databases Experience of delivering global clinical studies across different phases more »

Within pharmacy we have a position for a senior assistant technical officer. We are looking for an enthusiastic person to join our small pharmacy clinical trials team. We are responsible for ensuring that all the pharmacy and medicine aspects of clinical trials for cancers are conducted according to … daily basis providing feedback to relevant individuals as necessary. Management of IMP stock levels to include ordering, receiving, relabelling, archiving, according to Sponsor and GCP requirements To undertake routine expiry date checks and maintain the expiry date database. Arrange and act as a pharmacy representative at trial monitoring and close … field telephone calls and enquiries as appropriate. Person Specification Qualifications Essential NVQ 3/equivalent GCSE or equivalent passes in Maths, English and Science GCP training within last 2 years Desirable Excel and use of Microsoft office programmes Experience Essential Experience of using a variety of IT packages to include more »

bioanalytical study or other plans Team player Review and sign of study data Responsible for regulatory compliance as assigned Ensure all processes are following GCP/GLP Liaising with clients regarding within agreed timescales Qualifications At least 3 years experience working in a regulatory bioanalytical laboratory. A degree in life … sciences or chemistry-related subject A good communicator with strong interpersonal skills. Experience working within a GLP/GCP accredited facility. Flexible and adaptable with an eye for detail Hand-on experience of LC-MS/MS, Sciex and Waters LC-MS/MS systems is an advantage Experience more »

to improve the health and wellbeing of the people we care for, as well as supporting andempowering them to lead a fulfilling life. Our clinical teams deliver many NHS services, not only via inpatient and primary care settings, but also within the community. These services include children's, adult … Qualifications Essential Post graduate qualification in a field relevant to research A degree in law or equivalent qualification Desirable Evidence of continuing professional development GCP Trained Knowledge & Skills Essential Knowledge of clinical research governance Ability to communicate, negotiate and influence effectively as appropriate at all levels and be persuasive … Experience Essential Experience of working with contracts Experience of negotiating contracts in a life science or research setting Desirable Experience of working in a clinical research environment in an NHS Trust, University, pharmaceutical company, charity or other organisation Experience of analysing and interpreting complex contractual terms and/or more »

Hobson Prior is seeking a Biomarker Scientist to support clinical transcriptomics outsourced activities. The successful candidate will be responsible for conducting and supporting sample analysis, quality control, data interpretation, and reporting. This role requires staying updated with new and emerging techniques in the transcriptomics and biomarker fields. Please note … considered for this role you must have the right to work in this location. Key Responsibilities Act as a Subject Matter Expert in supporting clinical transcriptomics outsourced activities from planning and technical perspectives. Ensure timely delivery of high-quality, fit-for-purpose assays and robust data. Conduct and support … Experience of working with human tissue under the directives of the Human Tissue Act (HTA), and experience of working with samples and studies under GCP compliance. Practical experience in any of the following techniques would be an advantage: histology and immunohistochemistry, Immunoassay and ligand binding assays, Flow cytometry assays, LC more »

involved in NHS, academic and commercial research. The post involves high volume, face to face contact with patients, principally in the glaucoma service acquiring clinical diagnostic data to support and inform clinicians. The post holder interacts routinely with: patients, administrative, clerical, technical and clinical staff within the Trust … date professional development plan Desirable AOSP/ACHS Registration Previous technician certification for multicentre/international clinical trials Member Ophthalmic Imaging Association Current GCP Certification/NVQ 3equivalent Experience Essential Experience in ophthalmic imaging/retinal screening Evidence of recent professional development. Desirable Experience in a commercial photographic environment. more »