Empleos de start en 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 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...

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 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...

Study Start Up Associate I At 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...

Business Development Manager - Servicios de Reclutamiento (Remoto 100%) Únete a un equipo global en expansión líder en Servicios de Reclutamiento y Outsourcing Modelo de trabajo: Remoto 100% (para candidatos en cualquier ubicación de Latinoamérica, España, o USA) Disponibilidad: Jornada completa (lunes a viernes, 9 a 18 hs, fuull time) Modalidad:...

Study Start Up Associate IAt 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...

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...

ICON Strategic Solutions in Buenos Aires seeks a Study Start Up Associate I to drive site start-up and activation, ensuring regulatory compliance and timely initiation of trials within a sponsor-dedicated model backed by our global expertise.The role involves preparing regulatory documents, coordinating approvals, maintaining submission records, and...

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...

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...

IQVIA Biotech is seeking a Sr. Site Contracts Associate with 3–5 years of experience negotiating clinical site contracts and budget templates.The role focuses on developing global contracting strategy and supporting start-up contracting activities for selected sponsors and studies. Responsibilities include drafting grants and estimates, contract language,...

Lead, Regulatory Affairs, AMER, Amazon Leo RegulatoryDescriptionAmazon Leo is an initiative to launch a constellation of Low Earth Orbit (LEO) satellites that will provide low-latency, high-speed broadband connectivity to unserved and underserved communities around the world. This is a unique opportunity to work in the development of a global broadband...

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 smooth progression from feasibility and initial outreach...

Medpace Buenos Aires is seeking a full-time, office-based Site Contract Manager to join our LatAm Site Contracts team in Clinical Operations. You will report to the LatAm Senior Contract Manager and help drive study start-up and trial management.The role requires LATAM site contract expertise, knowledge of GCP, and English fluency. You will lead...

IQVIA LLC is seeking a Site Activation Specialist, ICF Lead to operate in LATAM on a remote basis. You will function as a senior individual contributor, coordinating site activation activities and ensuring compliance with local and international regulations, SOPs, and budgets.In this role you will manage feasibility, site identification, regulatory...

IQVIA LLC is seeking a Site Activation Specialist, ICF Lead to operate in LATAM on a remote basis. You will function as a senior individual contributor, coordinating site activation activities and ensuring compliance with local and international regulations, SOPs, and budgets.In this role you will manage feasibility, site identification, regulatory...

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...

Buenos Aires, ArgentinaFull timeRDescripción General del RolBrinda un aporte oportuno y de alta calidad al desarrollo de soluciones para proyectos orientados a service delivery, managed services o implementación para clientes.Las asignaciones suelen requerir análisis básico y resolución de problemas, con énfasis en cumplir los compromisos de entrega y...