specialist

We are currently looking for Drug Safety / PV Associate to join an international Clinical Research Organization, one of the top companies globally in this area. The successful candidate will be responsible for supporting drug safety, data management processes for quality of data processed, as well as performing any other support activities. Responsibilities: Providing support …

We are currently looking for Pharmacovigilance / Drug Safety Specialist, to join operations of a CRO company in Warsaw. The successful candidate will be responsible for preparing and submitting drug safety-related documents, as well as assessment of adverse event reports at local level. Responsibilities: Ensuring the survey and monitoring of national pharmacovigilance regulations, processing and …

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 …

We are currently looking for freelance or permanent Drug Safety / PV Officer to join operations of a pharmaceutical company in Finland. Preferred location is Helsinki, although we can consider candidates from other parts of region. The successful candidate will be responsible for preparing and submitting drug safety-related documents, as well as assessment of adverse …

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