1 to 9 of 9 Temporary Good Clinical Practice Jobs in England

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 »

interventional neuroradiology services. There will also be sessions in general diagnostic radiology to complement time in interventional radiology. Barts Radiology training programme has 50 clinical radiology trainees across the network. Candidates will be required to adhere to the Trust's policy on Maintaining Medical Excellence and to be committed … Health group of NHS hospitals is entering an exciting new era on our improvement journey to becoming an outstanding organisation with a world-class clinical reputation. Having lifted ourselves out of special measures, we now have the impetus and breathing space to chart a fresh course in which we … oFRCR oFull GMC registration. Experience Essential oEligible for specialist register in Radiology oRadiology SpR in an approved training post, or equivalent training oOr Previous Clinical fellow experience oDemonstrable commitment and enthusiasm for Interventional radiology., with previous experience oEvidence of recent CME/reasonable training progression at this stage of 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 »

Job summary The Liver clinical trials team at King's are inviting applications for a clinical trials data manager to work alongside the clinical trials team on an exciting portfolio of commercially funded and investigator led studies in liver diseases. The successful applicant will be an enthusiastic … . Responsible for the collection, co-ordination and computerisation of data generated from the clinical trials. Implement and adhere to the principles of GCP (Good Clinical Practice) as set out in the Clinical Trials Regulations. Liaise with and assist the medical team/sponsor organisation … . Responsible for the collection, co-ordination and computerisation of data generated from the clinical trials. Implement and adhere to the principles of GCP (Good Clinical Practice) as set out in the Clinical Trials Regulations. Act as a resource and support to patients and their 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 »

all the non-cancer non haematology beds, alongside the non resident general fellows. Main duties of the job Work closely and collaboratively with the Clinical Site Team, Modern Matrons, AHP and Nursing teams, as well as the ITU Fellows, Outreach team, Oncology Fellows and other Speciality Clinical Fellows. … Provide clinical support to the relevant Consultants, and be responsible for the clinical care of patients ensuring all in-patients on your allocated ward/s are reviewed daily and undertaking documentation, escalation when needed, as well as ensuring fluids/antibiotics etc are written up, and supporting … to audit, Quality Improvement workstreams, M&M, Risk, Complaints and Quality meetings and the reports/investigations that feed these meetings working with Divisional Clinical Director, Medical Director and Resident RMOs About us The London Clinic is one of the UK's largest private hospitals, where we pride ourselves more »

Training Essential Educated to degree level in relevant scientific discipline or equivalent Postgraduate qualification Experience/Knowledge Essential Regulatory requirements pertaining to ATMPs manufacture Good Manufacturing Practice and Good Clinical Practice Thorough understanding of gene and cell-based therapies Thorough understanding of HTA Proven experience … team Experience of using Q-Pulse Skills/Abilities Essential Writing and presentation of reports using computers Training and supervision of staff Personnel management Good organisational and leadership skills Strong communication skills (verbal and written) Strong problem-solving skills Ability to work independently and as part of a team … Good attention to detail and accuracy Desirable Project management Disclosure and Barring Service Check This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly more »