1 to 24 of 24 Good Clinical Practice Jobs in the UK excluding London

clinical trials of medicinal products and all aspects of pharmaceutical input in accordance with legal requirements and Good Clinical Practice (GCP) relating to the prescribing, handling, dispensing, administration, storage and disposal of investigational medicinal products (IMPs) advanced therapy investigational products (ATIMPs) and non - investigational medicinal products … Takes responsibility for the provision, management and development of a high quality, comprehensive specialist clinical trials pharmacy service 5.1. Works according to GCP guidelines and agreed pharmacy clinical trials procedures. 5.2. Critically appraises clinical trials protocols, including amendments, to assess feasibility and ensure all pharmaceutical aspects of … Pharmacy, or relevant postgraduate experience Demonstrates continued professional development or equivalent knowledge through extensive experience Awareness of Good Clinical Practice (GCP) Desirable Attendance at relevant regional and national Clinical trials courses/meetings Member of relevant specialist pharmacist group Current GCP certification. Teaching/Mentoring more »

and demonstrate that high quality data is being collected and that the trial is being conducted according to the ethically approved protocol and ICH-GCP standards. They will also coordinate data collection and data entry and responding to everyday queries from research nursing team and study participants including coordination and … delivery of a comprehensive, high-quality service within the CRF in accordance with Trust Policies, R&D SOPs, Good Clinical Practice (GCP) and all other regulatory requirements. *To contribute to the implementation, monitoring, improving and management of the CRF's Operations, policies and SOP and support its … in touch with the contact for this role. Person Specification Qualifications Essential Science graduate or equivalent level of Knowledge and experience Desirable Recent ICH GCP Training Experience Essential Experience of working in a clinical research environment within NHS, University or pharmaceutical industry Experience of working with multi-disciplinary teams. more »

progress research to improve patient care? We are looking for a hard-working, enthusiastic pharmacist who shares our Trust values to join our expanding clinical trials and research team at Mersey Care NHS Foundation Trust. Mersey Care is at the forefront of clinical trials for mental health, putting … of pharmacist as required3.Participation in screening, dispensing and checking of clinical trial prescriptions, and advising others of Good Clinical Practice (GCP), Good Manufacturing Practice (GMP) and requirements relating to Investigational Medicinal Product (IMP) management.4.To participate in the Trust-wide Out of Hours Medicines Advice … in Clinical Pharmacy, willingness to work towards or equivalent experience Registration with General Pharmaceutical Council Desirable Membership of the Royal Pharmaceutical Society (RPS) GCP training Knowledge/Experience Essential Demonstrable evidence of commitment to self development and CPD Experience of undertaking audit within pharmaceutical services Understanding of how medicines more »

policies and ensuring studies have all relevant approvals. In addition, you will play a key role in the performance, co-ordination and working alongside clinical teams in the set up of research studies. Attention to detail and the ability to work both as part of a team and autonomously … to name just a few. Job description Job responsibilities PRINCIPAL RESPONSIBILITIES To plan and coordinate your day-to-day work in collaboration with Senior Clinical Research Facilitator. To be responsible for robust and accurate data systems of research studies. Input to governance strategies. Support and assist in the development … appropriate understanding of the studies and trial documentation. To enter data onto the appropriate databases in relation to research governance studies. Work according to GCP and research governance standards for all aspects of work practice. Coordinate commercial studies under the supervision and support of senior colleagues. Adhere to research governance more »

Will be the Radio pharmacy expert and professional resource for the multi-disciplinary team. Ensure all Radio pharmacy work complies with statutory regulations and good practice codes; the latter including. The EU Guidance on Good Manufacturing Practice (GMP)/Rules and Guidance for Pharmaceutical Manufacturers and … pharmacy service, organising and implementing complex short, medium and long term plans in response to legislative and regulatory changes, infrastructure developments, evolving consensus of good practice and the availability of new diagnostic tests and treatments. About us Northampton General Hospital is one of the largest employers in the … room design, equipment and function. Understanding of Validation & Quality guidance including Design Qualification (DQ), Installation Qualification (IQ), Operational Qualification (OQ) and Performance Qualification (PQ) GCP knowledge and training RPS training Skills Essential Able to prioritise workload/flow of Leaders and team workers, methodical and organised, self-motivated and able more »

Job summary We are looking to appoint a consultant in Clinical Oncology with a special interest in the medical management of Gastrointestinal (GI), Neuroendocrine (NET) and Urological malignancies. The successful candidate will work with existing Medical and Clinical Oncology colleagues, clinical nurse specialists, nurse and pharmacist prescribers … job To provide a cancer service to patients with GI, NET and Urological malignancies throughout the trust and referral region. Maintenance of the highest clinical standards in the management of oncology To work with colleagues at Oxford University Hospital NHS Foundation To provide a cancer service to patients with … Communication skills should be highly developed Experience of teaching undergraduates and trainees Evidence of effective participation in clinical audit and risk management. ICH GCP training within last 12 months. Evidence of active involvement in clinical research trials. Desirable Management training and experience Knowledge of the organisation of the more »

Job summary We are offering an exciting opportunity for suitable applicants to join the pharmacy clinical trials team at the Sheffield Teaching Hospital NHS Foundation Trust. The Clinical Trials team is expanding its workforce to increase research at Sheffield teaching hospitals. The Trust is one of the busiest … to demonstrate knowledge of clinical trial processes, including relevant legislation and local policies (Band 6) Able to demonstrate specialist clinical trials knowledge (GCP,GMP), relevant or applicable to the job role, underpinned by theory or relevant practical experience (Band 5 & 6) Developed IT skills Desirable (Band 5) Able … to demonstrate knowledge of clinical trial processes, including relevant legislation and local policies (Band 5) Able to demonstrate specialist clinical trials knowledge (GCP,GMP), relevant or applicable to the job role, underpinned by theory or relevant practical experience (Band 5) Appropriate Short Management Courses e.g. Appraisal training, Leadership more »

Desirable *Appropriate professional qualification or knowledge of legal procedures and contracts gained through experience Experience Essential *Understanding of Good Clinical Practice (GCP) and the EU clinical trials directive *Knowledge of Common law of Confidentiality, Data Protection Act 2018 and GDPR. *Experience of report writing and managing …/analysing complex data. Desirable *In-depth understanding of clinical research and trial management methodology, including applicable regulatory requirements. *Significant Operational management experience working within a NHS environment working with clinicians and other health care professionals at all levels of the organisation *Writing Data Protection Impact Assessments (DPIAs) *HR … of normal office hours; *Ability to travel across all of UHB sites and to external sites if required. Desirable *Ability to propose changes to practice and lead on service development for specialist area, developing and implementing policy for that area. Propose changes in conjunction with service groups which have more »

resources available. You should be able to demonstrate experience of successfully managing an operational service as well as having recent experience of leading in clinical or research innovation and working in collaboration across professions and services. Sound knowledge and experience of genomics within maternity or paediatric services is desirable. … focus on a quality service which is all about people - patients, staff and partners. Recognised as providing 'outstanding' care to our patients and rated 'Good' overall by the Care Quality Commissioner, is testament to the skill and dedication of the people who work here. CUH's values - Together - Safe … Analysis, interpretation and use of information Time Management Able to react under pressure Knowledge Essential An understanding of issues surrounding research, including patient confidentiality, good clinical practice and research governance Comprehensive knowledge and understanding of NHS policy and strategy with a proven ability to translate into local more »

Job summary The post holder will lead the provision of a high quality, safe and effective pharmacy clinical trials service, to ensure compliance with the required National Standards and UHBResearch and Development Strategy. The post holder will be the Pharmacy Lead Facilitator for Research and Audit projects. They will … own professional actions and deliver a high quality specialisedclinical pharmacy service to promote the safe, rational and cost-effective use of drugs,through personal practice and the training of other staff. The post holder will contribute to the training and education for Undergraduate HealthProfessionals and Post-Graduate Pharmacists, Nurses … Health Board's Research & Development department and, supported by our highly experienced Senior Pharmacy Trials Technician, will provide expert regulatory knowledge with regards to GCP and pharmaceutical aspects of clinical trial delivery and management. The ideal applicant will be a highly motivated and methodical pharmacist who is able to more »

studies across all specialities. The team comprises of more than 50 dedicated and experienced members of staff this includes researchers, research nurses, research governance, clinical trials assistants and research support staff. Working in the research team, you will be joining a driven and caring department looking to enhance the … high-quality research sponsorship function. Provide expertise regarding research regulatory requirements, i.e., NHS Research Ethics Committee, HRA, MHRA, ICO, FDA, Research Governance Framework, ICH-GCP, and advise accordingly. Manage the development of systems which enable the recording and tracking of research approval and delivery timelines in accordance with institutional and … systems and structures. Ensure that all research carried out in the Trust complies with the UK Policy Framework for Health & Social Care Research, ICH GCP standards and best practice, including MHRA guidance. Advise on the development of research protocols and policies for RM&S and input into policies at more »

a meaningful impact on people's lives. Main duties of the job Why Join Us? At Likewise our Independent Prescribers are essential in implementing good clinical practices and pharmacological/health interventions. When you become a part of our team, you'll benefit from: Work/Life Balance … Flexible working hours to suit your needs. Clinical Support: Regular clinical supervision, appraisal, and revalidation support. Professional Growth: Generous CPD time to enhance your skills and knowledge. Leave Benefits: Generous annual leave entitlement (27 days, plus bank holidays, increasing to 32 after 1 year's service). Team … our impact reporthereto read more about the important work that we have done. Job description Job responsibilities Job purpose:To deliver drug and alcohol clinical and prescribing services to the service population. Key accountabilities: 1. Clinical assessment with or without Prescribing a range of medications (including controlled drugs more »

is also actively involved in NHS, academic and commercial research. The post involves high volume, face to face contact with patients, including those in clinical trials/academic research studies, to acquire clinical data through a wide range of ocular imaging procedures and other ophthalmic assessments, determined either … through standard operating procedures/research protocols or ordered specifically for individual patients by clinical staff. Results are interpreted by clinical staff and inform patient management decisions. The post holder interacts routinely with: patients, administrative, clerical, technical and clinical staff within the Trust and other external stakeholders … the line manager. For a full list of duties, please refer to the attached job description and person specification Person Specification Qualifications Essential Current GCP Certification/NVQ 3 equivalent Up to date professional development plan Desirable Basic level media qualification AOSP Registration Previous technician certification for multicentre/international more »

following SOPs: To co-ordinate the day to day workload, ensuring items are manufactured in a timely manner and colleagues are supported. To follow good manufacturing practice (GMP) at all times. To generate worksheets and labels, ensuring medicines are charged correctly using the pharmacy computer system. To in … Full Science Manufacturing Technician Level 3 Standard Registered Pharmacy Technician or Registered Science Manufacturing Technician Desirable Aseptic Preparation and Dispensing of Medicines Skills Essential Good communication skills Computer skills (dispensing, stock control) Use of Microsoft office applications, e.g. excel, word … Knowledge and Experience Essential In depth understanding of GMP. Knowledge of practice in hospital Aseptic Services Experience of final checking Desirable Experience of GCP/setting up clinical trials within an aseptic unit Experience of creating debtor forms, dealing with invoice queries. Experience of conducting risk assessments and more »

programme to the National Pathology Imaging Co-operative (NPIC). NPIC is now building on that advanced starting position, uniting a consortium of academic, clinical and industry partners with a common vision - to create a world-leading centre for digital pathology and artificial intelligence (AI) on which a UK … activities and strategic planning. Seek opportunities for reputational enhancement with Industry and drive new business opportunities and partnerships Manage a number of academic interdisciplinary clinical research projects, providing project manager level support, leading the clinical research delivery team and research fellows assigned to the projects to ensure on … Experience Project Database knowledge Experience Essential Demonstrable Knowledge And Understanding Of Medical Science Experience in developing and delivering research portfolio Substantial knowledge of ICH GCP and Research Governance ability to assimilate new knowledge and resolve and clarify complex and conflicting factors arising from research findings Research methodology Desirable Demonstrable Project more »

Responsibilities Participate in pre-clinical and clinical bioanalytical projects through method development, validations and routine sample analysis in accordance with GLP and GCP regulations. Experience of running LC-MS/MS and or LBS s including equipment maintenance and troubleshooting. Experience in running Ligand Binding Assays. Deliver projects … as part of a team Demonstrate knowledge of GLP/GCP and conduct all work in a manner that is compliant to regulatory requirements Qualifications and experience A degree in life science or chemistry-related field Hands-on experience with LC-MS/MS and Ligand Binding assays is desired … good communicator with strong interpersonal skills. Has a delivery focus with a good work ethic. Experience in working in a GLP/GCP accredited facility Knowledge of software-specific platforms is preferred Benefits Competitive Salary Pension Scheme Private Healthcare Generous Holiday Package Career Progression Opportunities more »

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over … processes in place. As an experienced CRA you'll be involved in initiation, routine & close out visits for studies in Phases II - IV of clinical development. Successful candidates will enjoy the benefits of working for a company that values work-life balance. Other Information: This role is a full … employed through Fortrea. For more information please contact Magdalena Koz owska, Recruiter at Key words: Clinical Research, SCRA, Clinical Research Associate, London GCP, Monitor, Monitoring, Senior Clinical Research Associate, CRA I, Oncology, Field Based, Home Based, CRO, Pharmaceutical, London Fortrea is actively seeking motivated problem-solvers and 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 »

capability for the handling of dangerous human pathogens and animal modelling of infectious diseases. The capability is used to understand pathogenesis and undertake pre-clinical development and assessment of new vaccines and therapeutics. The capability is also used to undertake studies in microbiological aerobiology, decontamination, and detection, and to … commercial projects on behalf of vaccine manufacturers. The Group has extensive experience in assay development and validation and operates to several Quality Systems including GCP, GLP and GMP. Main duties of the job Job description The purpose of this job is to perform routine duties related to and to provide … placements, or taught course Experience or understanding of working in a laboratory environment Experience or understanding of working within a regulated environment (e.g., ISO9001, GCP) and safe working practices Desirable Criteria Good knowledge and practical experience with specialist techniques for project i.e., working in a containment level 3 laboratory more »

Company description: QA Director Audit & Inspection GCP-CDCS As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across … process improvement initiatives What we offer: Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. more »

About the role 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 … large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-out investigational sites for clinical studies in phases II - IV, ensuring adherence to applicable regulations and principles of ICH-GCP. This position is multi-sponsor and supports medium and … in medicine, science, or equivalent Previous monitoring experience in medium and large -sized studies, including study start-up and close-out Knowledge of ICH-GCP guidelines and ability to review and evaluate medical data Excellent written and verbal communication Ability to work to tight deadlines Availability to travel (domestic fly more »

statistics/biostatistics Significant experience working within the clinical research/pharmaceuticals domain/Phase 3 Excellent knowledge of relevant regulations including ICH-GCP guidelines Proficiency with programming languages such as R/SAS/Python Strong communication skills, both written & verbal; ability to influence stakeholders at all levels more »

enthusiastic, self-motivated, organised quality professional with a keen eye for detail. Some previous experience (ideally between 1 - 2 years) of working in a GCP regulated environment or in a quality environment in a clinical trial organisation is desirable. Day to day, you will oversee the Companys quality systems more »

at Cambridge University Hospitals. The Data and AI Research Governance Coordinator is responsible for providing expert advice for a portfolio of research involving NHS clinical informatics and AI across a wide range of specialties, throughout the life course of the research project. The post holder will assist with the … initiative. We are an inclusive department and offer flexible working arrangements. Main duties of the job This post does not involve directly working with clinical data. The role holder will provide advice and support to researchers in all aspects of data and AI research governance, including submitting applications to … Knowledge and understanding of research funding streams and award bodies Qualifications Essential Educated to degree level or equivalent experience Desirable Post graduate research qualification GCP Trained Skills Essential Excellent communication skills Excellent organisational and planning skills Excellent interpersonal skills including the ability to build working relationships with department colleagues, Trust more »