Quality Assurance Manager - Europe

Remote Full-time
This a Full Remote job, the offer is available from: Europe The Manager of Quality Assurance is a quality professional within Linical responsible for assisting in the development and implementation of risk-based Good Clinical Practice oversight within Linical processes. This includes identification of risks, communication of risks to the organization, and working in a cross-functional team setting to mitigate the risks. Duties and Responsibilities β€’ Support the Quality Assurance department in maintaining Linical’s Quality Management System (QMS) for all Linical services including: β€’ Conduct of audits (systems, documents, TMF, clinical sites, vendors) β€’ Follow-up of corrective and preventative actions (CAPA) and deviations β€’ Supervision of SOP revisions β€’ Review of SOPs in cooperation with the operational staff to ensure compliance with GCP and regulatory requirements β€’ SOP-management (access control, notification of employees, tracking, etc.) β€’ Vendor qualification and management of related documentation β€’ Improving of standard and process for quality and efficiency β€’ Computer system validation/verification β€’ Provide support prior to and during regulatory inspections by authorities and audit performed by Sponsors on Linical β€’ Consultancy for operational staff in quality, procedural, and regulatory related questions β€’ Administrative tasks related to the maintenance of the QMS of Linical Required Skills and Abilities β€’ Excellent command of written and spoken English β€’ Ability to work independently and build strong, trusting working relationships with all departments and clients β€’ Skilled in advising team on quality and compliance matters β€’ Ability to familiarize oneself with specific indications, symptoms, and study designs β€’ Very good knowledge of standard office software Education and Experience β€’ University or college degree (or equivalent) in a medical or life-sciences related field β€’ Minimum 8-10 years experience in clinical research according to GCP with at least 2 years in a Quality Assurance role within a GCP-regulated environment β€’ Very good knowledge of GCP principles and related US, European, and other international regulatory requirements for the conduct of clinical trials β€’ Practical auditing experience β€’ Practical experience managing SOPs and the revision lifecycle This offer from "Linical" has been enriched by Jobgether.com and got a 81% flex score. Apply tot his job
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