startup start-up

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 the timelines agreed with project management and Site...

Department: Clinical Trial Operations, International OperationsLocation: Vicente López, Buenos Aires. Hybrid working.Your impact begins hereAs Study Start Up Analyst, you will help clinical trials in Argentina get started on time and the right way. You will prepare and submit the documents that Health Authorities and Ethics Committees need to approve a...

Premier Research is seeking a Senior Site Start up Associate to join our Clinical Monitoring, Site Management and SSU team. You will support global biotech and pharma sponsors by coordinating start-up activities, ensuring timelines, and maintaining regulatory alignment.You will work closely with Project Managers, Regulatory Start-up Managers, and local...

Premier Research is looking for a Senior Site Start up Associate to join our Clinical Monitoring, Site Management and SSU team. You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly connected to saving and improving lives,...

Job SummaryOur LATAM clinical trial activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Manager to join our Study Start Up team in Buenos Aires! This position plays a key role in the study start up process at Medpace. If you want an exciting career where you use your previous expertise and can develop...

Job SummaryOur LATAM clinical trial activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Manager to join our Study Start Up team in Buenos Aires! This position plays a key role in the study start up process at Medpace. If you want an exciting career where you use your previous expertise and can develop...

Job OverviewPrimary 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 the timelines agreed with project management and Site...

Job OverviewPrimary 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 the timelines agreed with project management and Site...

Premier Research is looking for a Senior Site Start up Associate to join our Clinical Monitoring, Site Management and SSU team.You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly connected to saving and improving lives, and...

Study Start Up Associate I - ArgentinaAt ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON's global expertise.As the world's largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that...

Medpace Overview Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical...

ICON Strategic Solutions is seeking a Study Start Up Associate I in Argentina to support site start-up and activation for clinical trials. You will collaborate with cross-functional teams to ensure regulatory compliance and timely study initiation, contributing to innovative therapies that benefit patients worldwide.The role emphasizes detailed regulatory...

Fortrea Argentina S.A. is seeking a Site Navigator II to coordinate site-level activities during the start-up phase of a clinical study.You will act as the single point of contact for investigative sites, ensuring regulatory compliance, training, and effective collaboration among sponsor, CRO, and site staff. Responsibilities include overseeing site...

Syneos Health in Argentina is seeking a Clinical Support Specialist to provide operational and administrative support across regulatory, study start-up and site activation functions. The role is based in a hybrid Argentina environment, collaborating with cross-functional teams to maintain project documentation, timelines and compliance.The ideal candidate...

Descripción Del Trabajo At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely...

Fortrea is seeking a Regulatory Affairs professional to act as the primary site liaison, ensuring timely collection and submission of essential documents for EC/IRB/Regulatory Authority approvals. You will support in-country regulatory activities, maintain compliant study documentation, and coordinate with vendors to meet global requirements.Experience with...

Medpace, Inc. in Buenos Aires is seeking a full-time, office-based Regulatory Submissions Manager to join our Study Start Up team in LATAM. The role focuses on managing global start-up activities, regulatory submissions, and ensuring quality of essential documents.The ideal candidate has at least 4 years of regulatory submissions/start-up management...

## Senior Site Start up AssociateApply: Remote: Argentina: Full time: Posted 25 Days Ago: R6338Premier Research is looking for a Senior Site Start up Associate to join our Clinical Monitoring, Site Management and SSU team.You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new...

IQVIA is seeking a delivery-focused professional to direct site activation, maintenance, and regulatory activities for selected studies or multi-protocol programs. You will define and oversee the scope of work, budget, and resources, ensuring timely execution and compliance across regions.The role includes providing regulatory and technical support to enable...

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 FunctionsOversee the execution of Site Activation (including pre-award/bid defense activities) and/or...