Regulatory Submissions Coordinator – Site Activation

Site Specialist IIICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.We are...

Who we areWe’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.We are Worldwide Clinical Trials, and we are a global...

Worldwide Clinical Trials in Argentina seeks a subject matter expert and local point of contact for regulatory submissions, site activation, and maintenance for awarded projects. You will plan, initiate, and track documents required for regulatory submissions, and ensure country requirements are met to achieve site activation goals.You will coordinate with...

Job SummaryJoin Medpace in our Buenos Aires office! As a Regulatory Submissions Coordinator you will have the opportunity to work within Regulatory Submissions, supporting our many projects and gaining some vital experience. You will be a productive member of the team, and will be mentored and supported as you develop your skills. Working directly with...

Site Specialist II ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers. We are...

Who we areWe’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence. We are Worldwide Clinical Trials, and we are a global...

Join Medpace in our Buenos Aires office! As a Regulatory Submissions Coordinator you will have the opportunity to work within Regulatory Submissions, supporting our many projects and gaining some vital experience. You will be a productive member of the team, and will be mentored and supported as you develop your skills. Working directly with Regulatory...

ICON plc in Argentina is seeking a site start-up and activation specialist to deliver high‑quality activation work, working closely with your team and stakeholders to drive study initiation.You will handle regulatory submissions, coordinate approvals, maintain submission records, and support study documentation, with travel up to 5% as needed.The role...

IQVIA is seeking a Clinical Trial Coordinator II to join our global delivery team. You will direct and manage site activation, maintenance and regulatory activities for selected studies, coordinating with Regulatory, Site Activation and project teams to ensure timely, compliant execution across regions.You will support pre-award activities, develop...