CRO

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 …

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 …

We are currently looking for (Jr) Drug Safety / PV Associate to join a leading global CRO initially for 6 months with a possibility to have a permanent contract. 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. …

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