Start-up Jobs in Argentina

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

IQVIA Biotech is hiring for Sr. Site Contracts Associate in with 3-5 years experience negotiating clinical site contracts and budget templates. Grant Plan a plus.IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience we offer agile therapeutical...

Job Overview:Site Navigators II plays a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical study and potentially through closeout activities as required. Serving as the single point of contact for investigative sites this role ensures...

Job OverviewDirect and manage the delivery of all required site activation maintenance and regulatory activities for selected studies or multi-protocol programs including pre-award activities oversight of the scope of work budget and resources.Essential Functions Oversee the execution of Site Activa...

Executive Assistant Extraordinaire: Transform Chaos into Success at Atlas AssistantsWe are looking for dedicated long-term partners for 100% remote Executive Assistants to support US-based clients.Successful candidates will be hired through Atlas Assistants and matched with a dedicated executive wit...

ROLE SUMMARYAs part of the Clinical Data Sciences (CDS) group an integral delivery unit within the Clinical Development & Operations (CD&O) organization the Head CDS Argentina is a key leader and influencer across Global Pfizer R&D on behalf of the CDS functions and the geography they represent. CDS...

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

Career CategoryClinical DevelopmentJob DescriptionJoin Amgens Mission of Serving Patients At Amgen if you feel like youre part of something bigger its because you are. Our shared missionto serve patients living with serious illnessesdrives all that we do.Since 1980 weve helped pioneer the world of b...

Job Overview:Coordinate and oversee aspects of logistics related to Clinical and Ancillary Supplies services. Support these services to both internal and external clients. Responsible for the set-up and coordination of project activities related to clinical and ancillary supplies. Independently supp...

Job Overview.Direct and manage the execution of the strategic operational and financial delivery of required Site Activation activities including but not limited to Site ID and Selection Ethics and Regulatory processes and Site Contracting for assigned studies as determined by Company scope of work...

This is an exciting opportunity to become part of a growing global pharma company focused on providing access to highly innovative therapies to patients in international markets. The ideal candidate embodies Medisons core values of Professionalism Trust & Mutual Respect Service & Cooperation Comp...

Overview:Were seeking a detail-oriented Vutek Operator to set up run and maintain large-format Vutek printers. Must have strong color skills mechanical aptitude and the ability to work in a fast-paced production environment.Key Responsibilities:-Set up and operate wide-format Vutek printers; load me...

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...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionPrepares reviews and coordinates under guidance and local EC submissions inalignment with global submission strategy. Supports preparation under guidance of local MoH submissions as applicable inalignment with global submiss...

Payroll & Accounts Payable SpecialistContract: Full-time Independent ContractorLocation: 100% remoteWorking hours: 40 hours per weekOur Firm:Sterlington is a full-service law firm that combines legal and commercial excellence with modern ways of practicing. Our high-caliber partners work on complex...

Payroll & Accounts Payable SpecialistContract: Full-time Independent ContractorLocation: 100% remoteWorking hours: 40 hours per weekOur Firm:Sterlington PLLC is a full-service law firm focusing on complex corporate litigation executive compensation and private wealth matters. As a firm we focus on t...

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...