Regulatory Documents Jobs in Argentina
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11 Jobs Found | Sort By : Relevance | Posted Date
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Site Readiness And Regulatory Specialist I
Fortrea
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...
Sr. Clinical Trial Coordinator
Thermo Fisher Scientific
Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionAccording to the specific role (Central or Local) coordinates oversees and completes functions on assigned trials activities detailed on the task matrix. - Performs department Internal Country and Investigator file reviews a...
Senior Clinical Research Associate
Psi Cro
We are looking for an experienced CRA ready to train and coordinate junior CRAs on site. Here you will have the opportunity to develop yourself as a trainer mentor and leader. We are committed to develop our employees in their careers by providing tailored courses and mentoring.Responsibilities will...
Clinical Research Associate I
Psi Cro
Hybrid position in Buenos AiresOnly CVs in English will be consideredWe are looking for a CRA to join our team in Argentina. Here you will have the opportunity to develop yourself as a senior trainer mentor and leader. We are committed to develop our employees in their careers by providing tailored...
Clinical Trial Coordinator Ii
Thermo Fisher Scientific
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 matrix.- Performs department Internal Country and Investigator file review...
Cra Sr Cra (sponsor Specific)
Fortrea
Summary of Responsibilities:Site management responsibility for clinical studies according to Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and Sponsor requirements including verification of study training records.Conducts site monitoring responsibilities for clin...
Site Activation Coordinator, Comex
Arg Iqvia Rds Argentina
Job OverviewThe Site Activation Coordinator will give support to Argentina in task related to import/export for site activation. Under general supervision perform tasks at a country level associated with site activation activities in accordance with applicable local and/or international regulations...
Senior Study Start Up Specialist, Iqvia Biotech
Iqvia
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...
Senior Study Start Up Specialist, Iqvia Biotech
Arg Iqvia Rds Argentina
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...
Fsp - Sr. Regulatory & Start Up Specialist
Arg Iqvia Rds Argentina
Job OverviewThe Sr. Regulatory & Start Up Specialist will perform 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 guidelin...
Fsp Sr. Regulatory & Start Up Specialist
Iqvia
Job OverviewThe Sr. Regulatory & Start Up Specialist will perform 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 guidelin...