Regulatory Submissions Jobs in Buenos Aires

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...

At Medtronic you can begin a life-long career of exploration and innovation while helping champion healthcare access and equity for all. Youll lead with purpose breaking down barriers to innovation in a more connected compassionate world.A Day in the LifeWere a mission-driven leader in medical techn...

Job descriptionThe Original Bitcoin ExchangeInspired by Bitcoins vision of financial freedom we are committed to empowering individuals to transact and connect seamlessly across the globe. From the early days of the Bitcoin revolution our mission has been to champion freedom through innovative relia...

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 Description Prepares reviews and coordinates under guidance local regulatory submissions (MoH EC additional special national local applications if applicable e.g. gene therapy approvals viral safety dossiers import license) in alignmen...

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...