Clinical Trials Jobs in Zagreb
Clinical Trials Jobs in Zagreb
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Job DescriptionThe Manager Regulatory and PV (Network) will assume leadership and functional representation for projects assigned and coordinate the local contact persons responsible for regulatory and pharmacovigilance activities. Job ResponsibilitiesAssume leadership and functi More...
The PV Associate should be a Pharmacist. This is an opportunity for new graduates to start and develop their career within drug safety. The PV Associate will be working as part of a project team performing and supporting contracted pharmacovigilance activities on behalf of PrimeVigila More...
Job DescriptionThe Manager Regulatory and PV (Network) will assume leadership and functional representation for projects assigned and coordinate the local contact persons responsible for regulatory and pharmacovigilance activities. Job ResponsibilitiesAssume leadership and functi More...
The Manager Regulatory and PV (Network) will assume leadership and functional representation for projects assigned and coordinate the local contact persons responsible for regulatory and pharmacovigilance activities.The Manager will also act as Local Contact Person for the designated More...
We are looking for a pharmacovigilance medical writer to join our team. The Medical Writer will be responsible for medical writing including:PSURs/PBRERsPADERsACOsDSURsRMPsQC and review of all written output from the operations team as requiredSupporting the project managers to More...
For the Client:To review and approve postmarketing Individual Case Safety Reports (ICSRs) and Serious Adverse Event (SAE) reports occurring in clinical trials for medical/causality assessment. The review includes coding seriousness assessment Company causality and comment listedness/e More...
At PrimeVigilance PV Officers are independent case processing team members who are expected to manage a variety of case processing services with full accountability. If you join PrimeVigilance you can expect to work with teams of different sizes from small clinical trial to More...
The PV Associate should be Pharmacist.This is an opportunity to start and develop your career within drug safety. The PV Associate will be working as part of a project team performing and supporting contracted pharmacovigilance activities on behalf of PrimeVigilance. If you More...
The PV Associate should be Pharmacist.This is an opportunity to start and develop your career within drug safety. The PV Associate will be working as part of a project team performing and supporting contracted pharmacovigilance activities on behalf of PrimeVigilance. If you More...
For the Client:To review and approve postmarketing Individual Case Safety Reports (ICSRs) and Serious Adverse Event (SAE) reports occurring in clinical trials for medical/causality assessment. The review includes coding seriousness assessment Company causality and comment listedness/e More...
Not Disclosed
The Medical Reviewer I is responsible for medical review of lCSRs and literature review writing of signal detection reports supporting writing and or reviewing of aggregate reports (DSURS PSURS/PBRERs/PADERS) as required by the Company or Client. Responsibilities include:To revie More...
The PV Associate should be Pharmacist.This is an opportunity to start and develop your career within drug safety. The PV Associate will be working as part of a project team performing and supporting contracted pharmacovigilance activities on behalf of PrimeVigilance. If you More...
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