.Precision for Medicine (CRO) are recruiting a Regulatory Manager to join our team. Candidates can be based in the following countries: UK, Spain, Hungary, Slovakia, Serbia, Romania or Poland.Position Summary:The Regulatory Manager (RM) provides regulatory strategy and development guidance for optimal conduct of clinical trials, regulatory agency meetings, orphan designations, paediatric planning, and accelerated procedures, ensuring timely preparation of well-organized, quality regulatory submissions in compliance with applicable regulations.The RM coordinates and prepares regulatory documents for submission to Regulatory Authorities and/or Ethics Committees, as applicable.The RM maintains a current knowledge of regulations and guidance documents, providing analysis to project teams, as well as supporting and enhancing Precision for Medicine's corporate Regulatory function.Essential functions of the job include but are not limited to:Provides regulatory guidance throughout the clinical development life cycle.Compile, coordinate and review applications to Regulatory Authorities including, but not limited to, CTA/IND, annual reports, routine amendments, scientific advice/regulatory authority meetings, orphan designations, paediatric planning, and marketing applications.Develops and/or reviews documents intended for submission to the Regulatory Authorities and/or Ethics Committees to assure compliance with regulatory standards.Serve as representative of Global Regulatory Affairs at project team meetings with both external and internal customers.Works within a project team, and where necessary, leads project for the region or globally.Oversee and coordinate Regulatory Affairs Specialists to achieve submission targets for contracted programs.Maintenance of project plans, project trackers and regulatory intelligence tools as it pertains to assigned responsibilities and to keep Regulatory Leadership updated.Assist in development of Regulatory Affairs Specialists and other operational area staff, as required.Provide input, as required, into regulatory strategy and timeline development for new study opportunities.Participates in maintaining and executing on the corporate quality initiatives across business units within clinical solutions.Keeps abreast and continually expand knowledge of laws, regulations and guidelines governing drug development and approval.Provides ICH GCP guidance, advice and training to internal and external clients.Serve as representative of Global Regulatory Affairs at business development meetings.Qualifications: Minimum Required:Bachelors degree, or equivalent experience, ideally in a scientific or healthcare discipline.5 years Regulatory experience required for the Manager level and 7 years Regulatory experience required for the Senior Manager Regulatory level.Computer literacy (MS Office / Office 365).Fluent in English.Preferred:Graduate, postgraduate.Possesses basic understanding of financial management
