Study Start-Up CRA: Site Monitoring & Regulatory Lead

ICON Strategic Solutions

Argentina

Presencial

ARS 1.200.000 - 1.800.000

Jornada completa

14 días+
Generador de candidaturas

Transforma esta oferta en una entrevista — un currículum y una carta de presentación creados pensando en lo que quiere el empleador.

Supera los filtros ATS

Ventajas ofrecidas por este puesto de trabajo

Competitive benefits

Descripción de la vacante

ICON plc in Buenos Aires seeks a Study Start Up Clinical Research Associate to oversee startup activities, ensure protocol compliance, and support site teams across trials. You will monitor sites, perform visits, and coordinate with cross-functional groups to ensure accurate data capture and regulatory adherence.

The ideal candidate holds an advanced degree in life sciences, nursing, or medicine, is based in Buenos Aires, and demonstrates strong English and regulatory/start-up experience in

Formación

  • Advanced degree required in life sciences, nursing, or medicine.
  • Based in Buenos Aires.
  • Advanced English required.
  • Strong experience in Regulatory Affairs for start-up projects.
  • Experience as a Clinical Research Associate with knowledge of trial processes.
  • Proficiency in monitoring, data integrity, and site management with clinical trial software/tools.

Responsabilidades

  • Monitor clinical trial sites to ensure adherence to protocol and GCP.
  • Conduct site visits, assess performance, and resolve issues for trial success.
  • Collaborate with cross-functional teams for timely data collection and reporting.
  • Provide training to site staff to maintain high trial conduct standards.
  • Build and maintain relationships with site personnel and stakeholders.

Conocimientos

Clinical Research
Regulatory Affairs (Start-up)
Site Management
Monitoring
Data Integrity
English Proficiency

Educación

Advanced degree in life sciences, nursing, or medicine

Descripción del empleo

ICON plc in Buenos Aires seeks a Study Start Up Clinical Research Associate to oversee startup activities, ensure protocol compliance, and support site teams across trials. You will monitor sites, perform visits, and coordinate with cross-functional groups to ensure accurate data capture and regulatory adherence.

The ideal candidate holds an advanced degree in life sciences, nursing, or medicine, is based in Buenos Aires, and demonstrates strong English and regulatory/start-up experience in

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