Senior Clinical Research Associate – Oncology Trials (Argentina)

Worldwide; Buenos Aires; Híbrido; ARS 1.200.000 - 1.800.000; Jornada completa

Descripción de la vacante

Worldwide Clinical Trials in Argentina is seeking an experienced Clinical Research Associate to oversee research activities at site locations, coordinating regulatory documents, contracts, budgets, and data reporting to ensure compliance.

The role involves initiating visits (SIVs), remote site management, and ensuring informed consent and safety reporting, with travel regionally as needed within Argentina.

Formación

• Excellent interpersonal, oral, and written communication skills in English.
• Superior organizational skills with attention to detail.
• Ability to work with little or no supervision.
• Proficiency in Microsoft Office, CTMS, and EDC Systems.

Responsabilidades

• Manage the research activities at sites participating in Worldwide’s clinical research projects.
• Identify potential sites, start-up activities, and contract/budget support; train sites to collect data.
• Conduct study initiation visits (SIVs).
• Ensure informed consent and safety reporting and regulatory compliance at all times.

Conocimientos

Interpersonal skills (English)

Organizational skills

Ability to work with minimal Superv.

MS Office proficiency

Educación

Bachelor's degree or Nursing Degree

Herramientas

CTMS

EDC Systems

MS Office

Descripción del empleo

Worldwide Clinical Trials in Argentina is seeking an experienced Clinical Research Associate to oversee research activities at site locations, coordinating regulatory documents, contracts, budgets, and data reporting to ensure compliance.

The role involves initiating visits (SIVs), remote site management, and ensuring informed consent and safety reporting, with travel regionally as needed within Argentina.