1 to 14 of 14 Good Clinical Practice Jobs in the North of England

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 »

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 »

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 »

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 »

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 … Fortrea is transforming drug and device development for partners and patients across the globe. Job overview: Provides strategic direction and oversight of Quality Assurance GCP Audit and Inspection operations and assures that audit program aligns with global RCQA strategies. Oversees external sponsor and inspectorate evaluations assuring follow up on trends … drive strategic business process improvement initiatives 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 »

inclusive of sample preparation, data acquisition and processing, and generation of development reports. ATTRIBUTES: A minimum of 3 years of study management experience in clinical and/or preclinical studies Strong background knowledge of … large molecule analysis in support of PK and PD studies. Experience working in a regulatory environment, managing studies that are compliant with GLP/GCP Experience in a client facing role with the ability to provide high level advice and guidance to clients Non-Smoker: due to the nature of 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 »

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 »

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 »

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 »

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 »

field of Data Sciences and Artificial Intelligence. This will be a supervised work theme exploring the use and analysis of big healthcare data for clinical decision making in emergency General Surgery as well as exploring the acceptability to patients of using healthcare data for research in Artificial Intelligence. The … successful applicant will work closely with the General Surgery, Colorectal and HPB surgical teams at Manchester Royal Infirmary as well as the Clinical Data Sciences Unit at MFT. The candidate will be expected to register for a higher degree with the University of Manchester which will be co-supervised … with all research governance processes as set by the MFT Research & Innovation Department Maintain an up-to-date Good Clinical Practice (GCP) in Research for the duration of the post The successful applicant will also be expected to register for the degree of MD/PhD at 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 »