Regulatory Documents Jobs in Argentina

Site Activation Coordinator Job OverviewUnder general supervision perform tasks at a country level associated with site activation activities in accordance with applicable local and/or international regulations standard operating procedures (SOPs) project requirements and contractual/budgetary guide...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Clinical Trial Coordinator 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 cou...

Job Overview:Primary contact with investigative sites during study maintenance and -when assigned- site startup activities with responsibility for collection of the required investigator and regulatory essential documents to ensure EC/IRB/Third body/Regulatory Authority submissions are made within t...

Job OverviewPerform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations standard operating procedures (SOPs) project requirements and contractual/budgetary guidelines. May also include maintenance activities.Es...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionAccording to the specific role (Central or Local) coordinates oversees andcompletes functions on assigned trial(s) activities as detailed on the task matrixPerforms department Internal Country and Investigator file reviews a...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionWe are currently seeking a Senior Regulatory Affairs Specialistto join our Regulatory Affairs department in Argentina. This is a fantastic opportunity to further develop your regulatory career and expertise in clinical trial...

Job Overview:Primary contact with investigative sites during study maintenance and -when assigned- site startup activities with responsibility for collection of the required investigator and regulatory essential documents to ensure EC/IRB/Third body/Regulatory Authority submissions are made within t...