8 Good Clinical Practice Jobs in the East of England

job The main purpose of the role is all set-up aspects of clinical trials, according to Good Clinical Practice (GCP), standard operating procedures (SOPs) and trust policies. The post holder will assist with the administration of clinical trials from feasibility to archiving including (but … complex workload activity with prioritisation, referring to the Research Manager as necessary.To have an understanding that all research must be conducted according to ICH-GCP, the EU Directive on Good Clinical Practice and the Research Governance Guidelines and assist the team in upholding these. About us At … computer skills, excellent oral and written communication skills. Attention to detail. Knowledge Essential Technical Professional Detailed knowledge of the clinical trials process and GCP guidelines/EU Directives Understanding of medical terminology. Disclosure and Barring Service Check This post is subject to the Rehabilitation of Offenders Act (Exceptions Order more »

Job summary Senior Assistant Technical Officer - Pharmacy Aseptic Services (Clinical Trials) We have an opportunity for a motivated and enthusiastic person to join our busy Pharmacy Aseptic Services - Clinical Trials Team. Do you have experience of working in a sterile production unit either within the NHS or Commercial … may have just the job for you! We are looking for a Senior Assistant Technical Officer with proven Aseptic skills and experience of dispensing Clinical Trial medications. In return we can offer a rewarding career pathway with the opportunity to undertake a Science Manufacturing Technician -SMT Apprenticeship (Level … in the Principles of Aseptic Pharmaceuticals Processing). Pharmacy Aseptic Services provides a range of sterile medicinal products including Chemotherapy, Total Parenteral Nutrition and Clinical Trial medications Our team is friendly and diverse and devoted to providing safe and timely products for our patients. Our services are an important more »

Job summary The Cambridge Clinical Trials Unit - Cancer Theme (CCTU-CT) is hosted by Cambridge University Hospitals (CUH) NHS Foundation Trust, which includes Addenbrooke's Hospital and is part of the Cambridge Cancer Centre, a partnership between Cancer Research UK, CUH and the University of Cambridge. As the Cancer … Theme of the Cambridge Clinical Trials Unit,we areresponsible for working with investigators to design, set up, conduct, analyse and publish cancer research studies sponsored by Cambridge University Hospital NHS Foundation Trust. The CCTU-CT currently accommodates both early and late phase studies, many addressing or associated with translational … scientific end points. We are seeking a trials data manager to be part of the cancer clinical trials team, which is part of the accredited Cambridge Clinical Trials Unit, to contribute to cancer research. We are looking for candidates with previous data management experience within a research environment. more »

Job DescriptionWorking as a Senior Quality Expert/Manager - GCP, you will act as the advisor to the Clinical Development teams on all quality related GCP activities. This will be an exciting opportunity with a clinical-stage biopharmaceutical company with multiple Phase 3 assets.Key Responsibilities:To play a … key role in maintaining and monitoring the GxP QMS ensuring it meets all regulatory requirements and standards, with emphasis on GCP compliance.To provide support and advice to Clinical Development teams with regards to:Definition of appropriate compliant procedures within GxP functionsManagement of quality issuesTo ensure external contracted organisations supporting … monitor the performance of GxP service providers with regards to the relevant quality standards.To define and manage clinical audit programme and to preform GCP audits if required.Maintain agreed quality metrics and dashboards to enable clear communication to senior management of compliance performance and any risks or issues identified.To maintain more »

Head of Clinical Data - Cambridge/London - Exciting MedTech Start-Up … Permanent + Tech-for-Good + Share options scheme Do you have a strong interest in the HealthTech and MedTech industry? Are you GCP trained with a Medical Degree and experience working in NHS? We’re looking for a Head of Clinical Data to join this exciting MedTech … universities Experience working in the NHS Experience working with data policies and GDPR Experience working with medical data contracts such as EHR and PACs GCP trained Great problem-solving abilities Excellent time management and communication skills What’s in it for you 💰: Competitive starting salary Share options scheme Hybrid working more »

debilitating disease areas. Our guiding principles, centred around Integrity and Patient-Centricity, are at the heart of everything we do. Job Purpose Lead all Clinical Data Management (CDM) lifecycle activities from protocol inception to database delivery for numerous global studies via oversight of multiple vendors and internal/external … database locks. Participates in Service Provider selection, evaluation and management, including reviewing and providing input to scope of work. Coordinates user acceptance testing for clinical databases. Contributes to global and sub functional working groups and initiatives. Responsibilities Responsible for delivery of clinical global study databases and specific study … is an essential part of the position Working as the sole Data Manager within the Team Key skills and experience In depth knowledge of GCP and current legislation. Working knowledge of Medidata Rave ( desirable but not essential) and IBM databases Experience of delivering global clinical studies across different phases more »

Job DescriptionHead of Clinical Data - Cambridge/London - Exciting MedTech Start … Up 🚀📢 Permanent + Tech-for-Good + Share options schemeDo you have a strong interest in the HealthTech and MedTech industry? Are you GCP trained with a Medical Degree and experience working in NHS?We’re looking for a Head of Clinical Data to join this exciting MedTech … start-up which aims to combine technology and medicine to improve the lives of patients who are dealing with complex diseases by using clinical data and Machine Learning technology. You’d be responsible for the data contracts that the company has with their partners as they run clinical more »

Assurance department. - Knowledge of GxP and Quality related regulations and standards within the Pharmaceutical/Medical Device industry. - Familiarity with ISO 9001, ISO 13485, GCP is essential. - Knowledge of ISO 21CFR Part 820, ISO17025, Clinical Trials experience, ISO13485 Lead auditor would be beneficial. Interested or know someone who might more »