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Keywords: Study Start Up Associate I (Regulatory Submissions) (Buenos Aires), Location: Buenos Aires

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Study Start-Up Associate I | Clinical Trials Onboarding (Buenos Aires)

A leading healthcare intelligence organization in Buenos Aires is seeking a Study Start Up Associate II. The selected... candidate will support site partners with regulatory submissions, manage document collections, and ensure compliance...

Company: ICON
Location: Buenos Aires
Posted Date: 15 Feb 2026

Study Start Up Associate I (Buenos Aires)

Overview Study Start Up Associate II ICON plc is a world-leading healthcare intelligence and clinical research... - Minimum of 1 year’s experience or understanding of clinical study start up requirements and activities. - Knowledge of local...

Company: ICON
Location: Buenos Aires
Posted Date: 15 Feb 2026

Study Start Up Associate I (Buenos Aires)

Study Start Up Associate II ICON plc is a world-leading healthcare intelligence and clinical research organization... - Minimum of 1 years’ experience or understanding of clinical study start up requirements and activities. - Knowledge of local...

Company: ICON
Location: Buenos Aires
Posted Date: 14 Feb 2026

Study Start-Up Associate I | Clinical Trials Onboarding

A leading healthcare intelligence organization in Buenos Aires is seeking a Study Start Up Associate II. The selected... candidate will support site partners with regulatory submissions, manage document collections, and ensure compliance...

Company: ICON
Location: Buenos Aires
Posted Date: 15 Feb 2026

Senior Director, Head of Argentina Clinical Data Sciences, Clinical Data Sciences (Buenos Aires)

management and study start-up, study conduct, and study close out activities - Review annual individual objectives.... They are accountable for all CDS activities, deliverables, and resources in their geography within CDS from planning through submissions...

Company: Pfizer
Location: Buenos Aires
Posted Date: 15 Feb 2026

Cra I, Cra Ii, or Senior Cra (Single-sponsor) (Buenos Aires)

in medium-sized studies, including study start-up and close-out - Knowledge of ICH-GCP guidelines and ability to review..., consent documents for ethics/IRB approval, as well as preparing regulatory submissions - Balancing sponsor generated queries...

Company: ICON
Location: Buenos Aires
Posted Date: 13 Feb 2026