LATAM Clinical Safety Coordinator - Pharmacovigilance

Medpace, Inc.; Buenos Aires; Presencial; ARS 97.979.000 - 135.663.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Office-based culture

Occasional WFH after training

Health benefits

Retirement plan

PTO benefits

Company social events

Descripción de la vacante

Medpace, Inc. is seeking a full-time, office-based Clinical Safety Coordinator to join our growing LATAM team in Buenos Aires. You will contribute to pharmacovigilance processes and collaborate with global cross-functional partners to ensure safety reporting and compliant documentation.

The role requires a life sciences degree, GCP knowledge, and fluency in Spanish and English, with 3 years of drug safety experience. This position offers on-site work with opportunities for professional growth.

Formación

• Bachelor's degree in life science is required.
• Fundamental knowledge of GCP guidelines and medical terminology.
• Knowledge of EDC systems and other clinical databases.
• Experience safety reporting to regulatory authorities in Latino LATAM Spanish-speaking countries.
• Drug safety experience.
• Knowledge of applicable safety reporting guidelines.
• Strong attention to detail.
• 3 years of experience in drug safety.
• Fluency in Spanish & English.

Responsabilidades

• Oversight of submission of safety reports to authorities in regulatory timelines.
• Regular interaction with Clinical Operations, Data Management and Regulatory Submissions.
• Draft study-specific safety documents as required.
• Work in a global team to distribute safety reports globally.

Conocimientos

Fluency in Spanish & English

Drug safety experience

Knowledge of GCP

Attention to detail

Safety reporting guidelines knowledge

Educación

Bachelor's degree in life science

Herramientas

EDC systems

Clinical databases

Descripción del empleo

Medpace, Inc. is seeking a full-time, office-based Clinical Safety Coordinator to join our growing LATAM team in Buenos Aires. You will contribute to pharmacovigilance processes and collaborate with global cross-functional partners to ensure safety reporting and compliant documentation.

The role requires a life sciences degree, GCP knowledge, and fluency in Spanish and English, with 3 years of drug safety experience. This position offers on-site work with opportunities for professional growth.