Study Start-Up Specialist II

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...

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...

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...

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...

Worldwide Clinical Trials in Argentina is seeking a regulatory start-up specialist to serve as the local point of contact for submissions, site activation and maintenance on awarded projects. You will plan, initiate and track essential documents to meet country requirements and site activation goals. You will coordinate country-specific patient information...

Medpace is seeking a full-time Contract Specialist to join the LatAm Site Contract Team within Clinical Operations. The role focuses on study start-up and management of site contracts with investigators and internal teams. You will prepare, negotiate and finalize CDA/CTA documents, budgets and LOI amendments, monitor timelines, and mitigate risks to...

Key Account Specialist (Rosario, Santa Fe) Descripción Del Trabajo Snapshot de la Posición: Ubicación: Rosario, Santa FeÁrea: VentasNegocio: Nestlé ProfessionalTipo de contratación: Full time permanenteFG I Objetivo del puesto: Desarrollar integralmente el negocio de Nestlé Professional en la zona asignada (Rosario, Sta Fe), siendo responsable por...

IQVIA Biotech seeks a Sr. Site Contracts Associate in Buenos Aires with 3–5 years of sponsor or CRO experience in site contracting. You will develop grant estimates, craft contract and payment language, and support global study startup activities while ensuring regulatory compliance. Join a leading CRO offering exposure to multi-protocol programs and...

Precision Medicine Group is seeking a Senior Regulatory and Start Up Specialist (Argentina), remote in Argentina. You will lead regulatory submissions, informed consent adaptations, essential document review, and support for site activation across the country according to local and international regulations. The role includes acting as SME for...