1 to 5 of 5 Temporary Good Clinical Practice Jobs in the UK excluding London

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 »

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 »

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 »

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 »

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 »