Permanent Good Clinical Practice Jobs in the East of England

5 Permanent Good Clinical Practice Jobs in the East of England

Senior Quality Manager - GCP

Ely, England, United Kingdom
Pharma Partners Recruitment Ltd
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 »
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Head of Clinical Data

Cambridge, England, United Kingdom
Hybrid / WFH Options
Oho Group Ltd
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 »
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Senior Data Manager

Cambridge, England, United Kingdom
Randstad Sourceright
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 »
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Head of Clinical Data

Ely, England, United Kingdom
Oho Group Ltd
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 »
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QA Officer

Cambridge, England, United Kingdom
Hobson Prior
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 »
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