05/06/2024 | Fulltime | Hillingdon | CV-Library | £46 - £48 / Hour Quality regulatory documents needed to support clinical trials and medical products. Contributing regulatory guidance in order to enhance product development As the regulatory lead, you will sit with the wider project team, providing guidance on how regulatory strategy should be implemented Ensuring
Save for laterRegister your CV05/06/2024 | Fulltime | Hillingdon | CV-Library | - £48 / Hour In the EU (inc. PIPs, variations, IMPDs, MAAs). Develops and implements regulatory strategy and executional plans and manages regulatory submissions (e.g., clinical trial and marketing applications) for assigned products in accordance with global filing plans, core labelling documents and regulatory
Save for laterRegister your CV21/05/2024 | Fulltime | Hillingdon | CV-Library | - £48 / Hour Considerations in developing strategy ensuring the regional needs are well defined and implemented in collaboration with relevant regional stakeholders. Manage regulatory submissions (e.g. clinical trial and marketing applications) for products in compliance with global filing plans and local regulatory
Save for laterRegister your CV20/05/2024 | Fulltime | Hillingdon | CV-Library | £46 - £48 / Hour Quality regulatory documents needed to support clinical trials and medical products. Contributing regulatory guidance in order to enhance product development As the regulatory lead, you will sit with the wider project team, providing guidance on how regulatory strategy should be implemented Ensuring
Save for laterRegister your CV15/05/2024 | Fulltime | Hillingdon | CV-Library | - £21 / Hour Experience and some knowledge and understanding of Clinical trial execution. Budget and project management experience preferred. Experience with Project Management tools and processes (e.g. MS Project, Excel, PowerPoint, Visio, MS Teams, SharePoint). Strong computer literacy, including word processing
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