Empleos de startup start-up en Buenos Aires

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 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...

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...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJob DescriptionJoin us as Start-up Team Manager - To manage complex site operations, ensure compliance with regulatory standards, support site recruitment and training efforts, and facilitate smooth collaboration between trial sites and internal teams to drive the success of clinical...

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 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...

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...

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...

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...

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...

Fortrea is seeking a regulatory submissions specialist to serve as primary contact with investigative sites, manage regulatory documents, and ensure timely submissions under ICH/GCP guidelines.The role involves coordinating with senior staff, vendors, and study teams to maintain compliance across country-specific requirements and prepare documents for...

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...

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...

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...

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 is seeking a Senior Site Activation Leader to drive global activation strategies for clinical trials across regions. You will oversee site identification, regulatory submissions, contracting, and lifecycle operations to meet timelines and stay compliant with ICH-GCP standards.Lead international projects, mentor teams, and manage budgets while...