Regulatory Submissions Jobs in Czech Republic

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Country Approval Specialist 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 across 100 co...

Job OverviewPerform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol applicable regulations and guidelines and sponsor requirements.Essential Functions Perform site monitoring visits (selection initiatio...

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...

Career CategoryRegulatoryJob DescriptionContract type: Amgen staff indefinite period fulltimeCZ&SK Affiliate Regulatory Head Sr Manager provides affiliate regulatory expertise and execution for the development registration and lifecycle management of all Amgen molecules.Job Summary:The Cluster Regul...

Career CategoryRegulatoryJob DescriptionThe Senior Associate in Regulatory Affairs supports country regulatory activities for the development registration and lifecycle management of all Amgen molecules. Contract type: Amgen Paid Temp - contract for 1 year fulltime jobReports to: Associate Director...

Regulatory Reporting FRA Analyst Own and execute daily / monthly production of FR 2052a FRY14 FRY15 liquidity reports ensuring completeness accuracy and timeliness. Prepare and validate FDIC regulatory reports in compliance with 12 CFR 369 (FDIC reporting requirements) and 12 CFR 370 (recordkeeping...

Job DescriptionThe Specialist Regional Submissions Planner will work within the our Global Regulatory Affairs and Clinical Safety (GRACS) organization in the Regional Regulatory Operations department (RRO) supporting regional planning activities for the EU EEMEA region while also contributing to cr...

Job DescriptionThe Senior Regional Submissions Planner will work within our Global Regulatory Affairs and Clinical Safety (GRACS) organization in the Regional Regulatory Operations department (RRO) supporting regional planning activities for the EU EEMEA region while also contributing to cross-regi...

Job DescriptionThe Senior Regional Submissions Planner will work within our Global Regulatory Affairs and Clinical Safety (GRACS) organization in the Regional Regulatory Operations department (RRO) supporting regional planning activities for the EU EEMEA region while also contributing to cross-regi...

Job DescriptionJob Description: Seeking a full-time Business System Associate Director for the Labeling Operations area within the GRACS Regulatory Innovation & Information Management organization.Primary area of responsibilities will include:Manage and lead Business Analysts for complex data analyt...

Cluster Expert for Medical Device Regulatory Affairs and VigilanceAt Fresenius Medical Care we are the global leader in kidney care committed to improving the lives of patients with chronic kidney disease. Our mission is to deliver high-quality innovative products services and care across the entire...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Clinical Trial Manager - Make an Impact at the Forefront of InnovationThe Clinical Trial Manager is accountable for achieving the final clinical deliverable (usually clean data from evaluable patients as specifi...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Sr Clinical Trial Manager/Clinical Trial Manager - Make an Impact at the Forefront of InnovationThe Clinical Trial Manager is accountable for achieving the final clinical deliverable (usually clean data from eva...

Clinical Research Associate Your responsibilities will include:Performing site selection initiation monitoring and close-out visitsSupporting the development of a subject recruitment planEvaluating the quality and integrity of site practices in accordance with regulatory requirements i.e. Good Clini...

Clinical Research Associate Your responsibilities will include:Performing site selection initiation monitoring and close-out visitsSupporting the development of a subject recruitment planEvaluating the quality and integrity of site practices in accordance with regulatory requirements i.e. Good Clini...