Associate I, TMF Operations

, creative approaches and implement them with quality and excellence. We are WorldwideClinicalTrials, and we are a global... Standard Operating Procedures, country-specific regulations, and industry best practices. Throughout WorldwideClinicalTrials...

Lugar: Argentina | 29/07/2026 21:07:09 PM | Salario: S/. No Especificado | Empresa: Worldwide Clinical Trials

Regulatory Affairs Officer , IQVIA Biotech

, guidelines, and agency expectations for clinicaltrials. · Demonstrated expertise in at least one clinical trial regulatory... writing and submission publishing. · Draft, review, and quality-check clinical trial regulatory core study documentation...

Lugar: Buenos Aires | 28/07/2026 21:07:26 PM | Salario: S/. No Especificado | Empresa: IQVIA

Regulatory Affairs Officer, IQVIA Biotech

, guidelines, and agency expectations for clinicaltrials. · Demonstrated expertise in at least one clinical trial regulatory... writing and submission publishing. · Draft, review, and quality-check clinical trial regulatory core study documentation...

Lugar: Buenos Aires | 10/06/2026 23:06:43 PM | Salario: S/. No Especificado | Empresa: IQVIA