CRO

We are currently looking for Pharmacovigilance / Drug Safety Specialist, to join operations of a CRO company in Belgium. 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 …

Our Client is an international Clinical Research Organization, one of the top companies globally in this area. As a result of their growing business, they are looking for a Senior Director of Patient Safety to support and drive strategic and operational functions of the Pharmacovigilance and Patient Safety business in Germany or UK. Responsibilities: Perform …

Our Client is a rapidly growing international Clinical Research Organisation offering an experienced (Senior) CRA opportunity to work from home on full FTE as part of their team in Spain. Responsibilities: Conducting start-up activities and monitoring visits Maintaining study files, writing clinical trial reports and liaising with vendors Reviewing progress of projects and initiating appropriate actions to achieve …

Our Client is a rapidly growing international Clinical Research Organisation offering an experienced (Senior) CRA opportunity to work from home on full FTE as part of their team in Italy. Responsibilities: Conducting start-up activities and monitoring visits Maintaining study files, writing clinical trial reports and liaising with vendors Reviewing progress of projects and initiating appropriate actions to achieve …

My Client are an international Clinical Research Organization, one of the top companies globally in this area. As a result of their growing business, they are looking for a new Medical Director who will focus on clinical development in the area of dermatology in phases II-III of clinical trials. Responsibilities: Provide internal and external partners …

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