Senior Clinical Research Associate - Lead On-Site Trials

IQVIA; Buenos Aires; Presencial; ARS 1.800.000 - 3.000.000; Jornada completa

Descripción de la vacante

IQVIA is seeking a Senior Clinical Research Associate to oversee planning, execution, and management of clinical trials. Responsibilities include site visits, recruitment planning, protocol training, and ensuring data integrity and regulatory compliance.

The role requires strong organizational skills, ability to work independently, and travel as needed. Proficiency in CTMS/EDC and English language is essential.

Formación

• Bachelor's degree in a health care or science discipline or equivalent.
• At least 4 years of on-site monitoring experience.
• Advanced in English.
• Knowledge of GCP/ICH guidelines and regulatory requirements.
• Strong organizational and time management skills.

Responsabilidades

• Perform site selection, initiation, monitoring and close-out visits with proper documentation.
• Support development of subject recruitment plans.
• Establish regular communication and train sites on protocol and study procedures.

Conocimientos

On-site monitoring

GCP/ICH knowledge

Advanced English

CTMS proficiency

EDC proficiency

Independent worker

Team collaboration

Educación

Bachelor's degree in health care or sciences

Herramientas

CTMS

EDC

Descripción del empleo

IQVIA is seeking a Senior Clinical Research Associate to oversee planning, execution, and management of clinical trials. Responsibilities include site visits, recruitment planning, protocol training, and ensuring data integrity and regulatory compliance.

The role requires strong organizational skills, ability to work independently, and travel as needed. Proficiency in CTMS/EDC and English language is essential.