manager

On behalf of our Client who are an International Pharma Group, we are looking for an experienced Regulatory Affairs Specialist to join their team in Spain. In this role you will report to Head of Regulatory Affairs. Responsibilities: Preparing EU submissions and submitting regulatory dossiers Setting strategies for European branded generic drug registrations Monitoring, preparing …

On behalf of our Client who are a global pharma company we are looking for a (Senior) Clinical Data Manager who will be responsible for data management and working as a part of a project team. Responsibilities: Data collection and management of multiple clients Responsibility for consistent study data documentation as well as for writing …

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