1 to 25 of 37 Good Clinical Practice Jobs in the UK excluding London

Job summary An exciting opportunity has arisen for a Specialist Clinical Trials & Cancer Services Pharmacist to join the Cancer and Aseptic Services team at ESHT. The successful candidate will lead on a portfolio of cancer & non-cancer clinical trials undertaken … within ESHT. They will appraise all relevant clinical trials & offer pharmaceutical input in accordance with legal requirements & Good Clinical Practice (GCP) relating to the prescribing, handling, dispensing, administration, storage & disposal of investigational medicinal products (IMPs) & non-investigational medicinal products (NIMPs). They will also contribute to … the delivery of a high quality specialist clinical pharmacy service to cancer clinical services. Experience in Cancer &/or Aseptic Services is essential. They will not only have the opportunity to explore & enhance their clinical expertise, but will also be developing management, training & leadership skills. They will more »

us You will join a small pharmacy-based team, where you will help to ensure the standards of Good Clinical Practice (GCP) are followed and that patients who volunteer to take part in clinical trials feel valued and receive an excellent pharmacy service. You will work … Operating Procedures (SOPs). To prepare invoice requisitions for clinical trial fees and monitor the receipt of income for specific trials. To attend GCP training as required by the Trust and to work to GCP standards at all times. To attend meetings regarding the set up and running of … Level 3 Pharmacy Services, BTEC Pharmaceutical Sciences or equivalent Registered Pharmacy Technician with the General Pharmaceutical Council Accredited Checking Pharmacy Technician (ACPT) qualification Desirable GCP training Skills and Experience Essential Good understanding of Clinical Trials Experience of working in a hospital pharmacy Evidence of working in a team 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 »

Manchester Childrens Hospital. As the Paediatric BMT Data Manager you will be responsible/for the high quality capture, processing and submission of complex clinical data from clinical systems within the Trust, ensuring the data is handled in a timely manner in line with EBMT recommendations. This includes … Operating Procedures (SOPs) with respect to the Data Protection Act, the Freedom of Information Act and ICH Good Clinical Practice (ICH GCP). To work alongside other Data Managers and Data administrators with the data entry and configuration tasks necessary to support the BMT Electronic Database (Access … Operating Procedures (SOPs) with respect to the Data Protection Act, the Freedom of Information Act and ICH Good Clinical Practice (ICH GCP). To work alongside other Data Managers and Data administrators with the data entry and configuration tasks necessary to support the BMT Electronic Database (Access more »

Job summary Are you an enthusiastic individual who is looking for a new challenge in Clinical Research? Do you want to make cutting edge clinical research available to a wider range of people? Do you have an inquisitive mind? If so, we would like to hear from you … our team for 12 months . A secondment is possible, if approved by your current manager. BCHFT is a Mental Health Trust, and our Clinical Research portfolio of studies covers all services, including Eating Disorders, LearningDisability, Memory Assessment, IAPT, Early Intervention, Autism and many more. Main duties of the … manage workload Desirable Awareness of clinical research governance issues, including risk management, and ability to resolve queries Good Clinical Practice (GCP) knowledge Skills/Personal qualities Essential Excellent spoken and written communication skills, including the ability to articulate information concisely, accurately and accessibly Ability to develop more »

Clinical Data Manager – £35,000-£47,000 per annum– Liverpool/Hybrid The Role Do you have a keen eye for detail and a knack for ensuring data accuracy? Are you excited about using cutting-edge AI to transform healthcare? MyCardium AI, a rapidly growing company using AI to … revolutionise cardiac MRI analysis, is seeking a highly motivated Clinical Data Manager to join our team in Liverpool. In this pivotal role, you will oversee the collection, management, and analysis of imaging data from clinical trials. You'll ensure data quality and integrity, working closely with a dynamic … clinical data management, ideally in imaging. Experience with imaging data and software (PACS, DICOM). Knowledge of Good Clinical Practice (GCP) and regulatory guidelines. Proficiency in data management software and databases. Strong understanding of clinical trials and regulations. Excellent organisation and communication skills. Ability to more »

Senior Clinical Biochemist STATUS: Full Time LOCATION: Onsite in Yorkshire, England DEPARTMENT: Laboratory SCHEDULE: Tuesday to Saturday; Day Shift SUMMARY As a seasoned Scientist IV in Clinical Biochemistry, you will play a vital role within our Laboratory team. … Your responsibilities encompass the meticulous analysis of clinical samples across automated and manual platforms, adhering strictly to Good Clinical Practice (GCP) standards. Joining our esteemed international organization offers more than just a job — it's an opportunity for professional growth and development. Supported by visionary leadership … empowering you to shape our organization and chart your career trajectory. ATTRIBUTES: • BSc in Biomedical Sciences or equivalent. • Minimum of 6 years' experience in clinical biochemistry. • Proven expertise and proficiency in assays/platforms within the laboratory setting. KEY RESPONSIBILITIES Analysis: Conduct thorough analysis of clinical trial samples more »

a super exciting pharmaceutical startup client based in Oxford. They are looking for someone to come and drive Good Clinical Practice (GCP) principles, who can come in and build relationships with key stakeholders in order to keep the quality team moving forward. The ideal person will have … strong QA experience within pharma and GCP, someone who is willing to be hands-on and into the detail expected when operating within a startup environment. This individual will also be a fantastic communicator, comfortable dealing with senior leadership and presenting up to that level. Responsibilities: Ensuring GCP is maintained … senior leadership and represent QA in reporting What you will bring: Previous project management experience within pharma/biotech or similar Outstanding knowledge of GCP, TFA and FDA regulations Strong project management principles, key knowledge of agile methodology A desire to be hands-on and into the thick of things more »

Quality Assurance Manager - Good Clinical Practice Our client, based in Cheshire are recruiting for a contract GCP QA Manager to join them for a 6 month project. This is an exciting opportunity to join a dynamic company with a great culture. Role: Provide strategic direction for quality … CAPA Process to ensure effectiveness Support the development of a risk based audit programme Maintain network of external audit providers to support CMC, pre-clinical and clinical activities. Support the management, implementation, and maintenance of the Quality Management System to support clinical development … activities. Support senior management in providing direction and leadership to staff to ensure a quality mindset is embedded in the business Requirements: Expert in GCP with working knowledge of GMP 5 years experience in a QA Manager role within a CRO, Biotech or Pharma company Contract: Hours: 3 days a more »

Job summary Applications from a variety of different clinical/professional backgrounds are invited, including Nursing, AHPs, Psychology, etc. All applicants must be able to demonstrate that they meet the essential criteria. We have a fabulous opportunity to join Derbyshire Healthcare's Research and Development team based at the … invited for a fixed term contract opportunity to end of FY 24/25, with potential for extension beyond, for a Band 6 Lead Clinical Researcher/Research Nurse/Research OT (depending on the applicant's professional/clinical background) role, based within the Centre for Research … and Development at Derbyshire Healthcare NHS Foundation Trust.If you want to gain research experience by using your clinical skills to support the delivery of high quality nationally funded research focused on improving patient care in the NHS, please apply. "It is Trust policy that for posts that are for more »

work in a multidisciplinary environment Effective verbal and written communication skills Understanding of principles of audit and clinical governance Desirable Previous audit completed GCP certificate of Good Clinical Practice Communication Essential Demonstrable skills in written and spoken English that are adequate to enable effective communication about more »

Associate Director of GCP | Permanent | Hybrid - Oxford | Circa £95k We are currently working on a new Associate Director of Good Clinical Practice position at a super exciting pharmaceutical startup client based in Oxford. They are looking for someone to come and and be the right-hand person … deputising for them, sharing responsibility and leading the team when required. The ideal person will have strong QA and managerial experience within pharma and GCP, someone who is willing to be hands-on and into the detail expected when operating within a startup environment. Responsibilities: Ensuring GCP is maintained and … to senior leadership and represent QA in reporting What you will bring: Roughly 7+ years working in a leadership QA position Outstanding knowledge of GCP, TFA and FDA regulations Strong management skills A desire to be hands-on and into the thick of things Logistics: Salary of around more »

regulations, and guidelines within the NHS or relevant healthcare setting. Familiarity with relevant legislation, such as the Human Tissue Act, Data Protection Act, and Good Clinical Practice guidelines. Excellent communication skills, including being able to communication highly sensitive and complex issues to managers and staff. Ability to … are achieved. Desirable Possess highly developed, specialist knowledge related to research activity/research governance. Continuously updates specialist knowledge relating to research governance, ICH GCP guidance and UK directives. Knowledgeable of current, potential research and information relevant to the care of patients within specialist clinical areas and relevant to … clinical trial participation. Excellent IT skills, ITQ/ECDL or knowledge through broad experience. In depth knowledge of NHS organisations and the challenges they face. Experience Essential Extensive background in roles closely tied to research, innovation, or a pertinent scientific field, showcasing substantial expertise. Proven proficiency in research processes more »

in a variety of research across numerous specialties. The role is working collaboratively with the clinical team to deliver hosted studies to ICH GCP standards. The successful candidate will be responsible for all aspects of clinical trials data management, playing a key role in the organisation, co-ordination … and execution of all aspects of clinical research data management and administration, including maintaining site files and accurately entering data into case report forms and IT based systems. This role involves working in collaboration with patients, research teams, hospital departments, other NHS Trusts, commercial and academic partners. You will … be required to work across the research portfolio under the supervision of our clinical trials team. Excellent attention to detail, ability to multitask and organise workload are essential skills for this post. There is the opportunity for progression to a Band 3 within this role upon completion of stipulated 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 »

Job summary We are looking for a dynamic and enthusiastic clinical pharmacist, looking to expand their knowledge and experience in clinical trials. If you have not worked in clinical trials before but would like to gain experience, then please apply. You will join a high-profile dedicated … healthcare professionals and other agencies relating to pharmaceutical aspects of clinical trials. To understand EU and UK Clinical Trial legislation relating to GCP, GMP and medicines management and ensure incorporation into the implementation of new clinical trials. To deliver specialist education and training in Clinical Trials … risk assessments. To work with and support the pharmacy team working within clinical trial implementation at UHCW. Assisting the team undergoing statutory MHRA GCP inspections and implement corrective or preventative actions. Assisting the development of policies, guidelines, audits and research relating to the use of medicines and devices within more »

exciting and growing Biotechnology company based in Oxford and am assisting them in a search for an Associate DIrector of Clinical Quality Assurance (GCP). The successful candidate will be reporting directly to the Head of QA and spearhead all activities related to GCP. Main Duties and Responsibilities include … Ensuring changes in GCP practices are communicated, adopted and implemented throughout the organisation by maintaining current knowledge of local and international regulations To create/author/approve or input into SOPs and policies for those relating to GCP activities To provide GCP training for staff including the preparation of … and delivery of training. To include onboarding/induction training and refresher training To take a lead role on behalf of QA on all GCP investigations including serious breaches and Urgent Safety Measures and to communicate these effectively within the organisation and escalation to the senior leadership team To represent 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 »

bioanalytical studies. 3. A working knowledge and practical experience using LC-MS/MS. Key Words: Small Molecule | Study Manager | Team Lead | Bioanalysis | GLP | GCP | Method Development | Validation | Sample Analysis | Regulatory Compliance | LC-MS/MS Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by more »

responsibility for duties including: Designs and oversees the implementation quality management systems for CMC development activities including the release of product for GLP and GCP studies. Provides quality expertise in accordance with the global quality requirements in the creation of product characterisation, product specifications, method validation, stability and comparability assessments … in the collaboration with C(D)MOs. Ensures that there are robust processes in place for the review and release product for GLP and GCP studies. Ensures appropriate quality oversight of GMP activities performed by the Product Development teams at Dechra or CDMOs and contract laboratories. This may include review more »

work within the team. The post holder must ensure a high standard of project execution, adhering to research protocols and project proposals across various clinical specialties. This role is both challenging and diverse, working within a growing team that has multiple priorities. The candidate must possess excellent organisational skills … work within the team. The post holder must ensure a high standard of project execution, adhering to research protocols and project proposals across various clinical specialties. This role is both challenging and diverse, working within a growing team that has multiple priorities. The candidate must possess excellent organisational skills … with MS Office (particularly Excel) applications. Understanding and experience of research lifecycle. Understanding of research management systems. Awareness of Principles of Data Protection and Good Clinical Practice. Demonstrate a clear understanding of confidentiality. Experience of working in a busy environment working independently and exercising judgement and decision-making more »

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 »

research facilitators who will take responsibility for the smooth set-up of research across the trust. The role forms an essential bridge between investigators, clinical teams and funders, building accurate and comprehensive grant application costings and working through timely study set-up and delivery. This role will ensure the … largest acute teaching Trusts in England, we offer learning and development opportunities to help you achieve the career you aspire to. UHS is rated 'Good' by the CQC and in the latest national NHS Staff Survey, we were in the top 10 acute trusts for staff engagement and for … of the set-up or delivery of clinical research in a healthcare setting. Experience of delivery training Evidence of current and on-going GCP training Project management experience Knowledge of research governance and quality assurance systems to ensure safe systems for patients An understanding of current R&D issues 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 … Experience may be substituted for education. 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 »

the sourcing, procurement and supply of unlicensed Medicines in line with National Guidance To help network with other Trust pharmacy departments to share best practice To contribute pro-actively to regular weekly team meetings to encourage staff ideas, service improvements and patient safety. Analytical Skills Help ensure statistical information … Head of Pharmacy/Chief Pharmacist as appropriate, when required. To assist with reporting on any current and future (horizon scanning) changes in prescribing practice and report on how this change in practice may affect the drug budget. Help ensure the recording of any drug defects (and sending … followed with patient identifiable data Responsibility for research and development To be authorised to receive and confirm receipt of clinical trial medication following GCP guidance and ensure that relevant records/information is documented and stored . Person Specification education and training Essential oRegistered Pharmacy Technician with GphC Experience more »