Clinical Research Associate - Freelance (Buenos Aires)

, and applicable regulatory requirements. The CRA will support study sites throughout the clinical trial lifecycle including initiation... according to protocol, GCP, ICH guidelines, and applicable regulatory requirements Review source documentation and Case Report...

Lugar: Buenos Aires | 27/02/2026 18:02:52 PM | Salario: S/. No Especificado | Empresa: TFS HealthScience

Clinical Research Associate - Freelance

Clinical Practice (GCP), ICH guidelines, and applicable regulatory requirements. The CRA will support study sites throughout..., and close out visits Ensure clinical trials are conducted according to protocol, GCP, ICH guidelines, and applicable regulatory...

Lugar: Buenos Aires | 27/02/2026 18:02:28 PM | Salario: S/. No Especificado | Empresa: TFS HealthScience

Clinical Research Associate - Freelance (Buenos Aires)

Clinical Practice (GCP), ICH guidelines, and applicable regulatory requirements. The CRA will support study sites throughout..., and applicable regulatory requirements - Review source documentation and Case Report Forms (CRFs) to ensure accuracy, completeness...

Lugar: Buenos Aires | 27/02/2026 18:02:59 PM | Salario: S/. No Especificado | Empresa: TFS HealthScience

Clinical Research Associate - Freelance

Clinical Practice (GCP), ICH guidelines, and applicable regulatory requirements. The CRA will support study sites throughout..., and close out visits Ensure clinical trials are conducted according to protocol, GCP, ICH guidelines, and applicable regulatory...

Lugar: Buenos Aires | 26/02/2026 22:02:23 PM | Salario: S/. No Especificado | Empresa: TFS HealthScience