Safety Reports Jobs in Czech Republic

Work ScheduleOtherEnvironmental ConditionsOffice Some degree of PPE (Personal Protective Equipment) required (safety glasses gowning gloves lab coat ear plugs etc.) Will work with hazardous/toxic materialsJob DescriptionConducts multiple ongoing clinical trials of varying size and complexity involvi...

Safety Specialist - Data Analysis & ReportingLocation:Columbus Central Services - Columbus MTSchedule:5x2 4x3 9hr ShiftsJob Responsibilities and Duties:At Sibanye-Stillwater the Safety Specialist is responsible for providing safety leadership and safety guidance to all employees. The Safety Speciali...

For the Client:To review and approve post-marketing 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/expectedness an...

For the Client:To review and approve post-marketing 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/expectedness an...

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 large generic post-marke...

The PV Assistant - Danish language speaker will be working as part of a project team performing and supporting contracted pharmacovigilance activities on behalf of PrimeVigilance. Previous work experience in pharmacovigilance is not required as you will receive all necessary training from us. If you...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as an Assistant Clinical Research Associate Make an Impact at the Forefront of InnovationWe have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs spanning 2700 clinical trials ac...

Job DescriptionJob Description - Clinical Safety and Risk Management Associate Principal ScientistThe Clinical Safety and Risk Management Medical Associate Principal Scientist performs primary medical review of serious adverse experience (AE) reports and other AE reports of interest in order to moni...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionConducts multiple ongoing clinical trials of varying size and complexity involving patients or healthyvolunteers/subjects. Completes all paperwork required to capture all data as specified by a studyprotocol and for ensuring...

Job Description:We Dream. We Do. We Deliver.As afull-service data-driven customer experience transformationwe partner with Top 500 companies in the DACH region and in Eastern Europe. Originally from Switzerland Merkle DACH was created out of a merger Namics and Isobar - two leading full-service digi...

Job Description:We Dream. We Do. We Deliver.As afull-service data-driven customer experience transformationwe partner with Top 500 companies in the DACH region and in Eastern Europe. Originally from Switzerland Merkle DACH was created out of a merger Namics and Isobar - two leading full-service digi...