CRA Senior en Ensayos Clínicos — Monitoreo y Regulatorio

Acerbrag; Buenos Aires; Presencial; ARS 139.086.000 - 185.448.000; Jornada completa

Descripción de la vacante

IQVIA in Buenos Aires, Argentina, is seeking a Senior Clinical Research Associate to oversee site monitoring, data integrity, and regulatory compliance across multicenter clinical trials.

You will perform site selection, initiation, monitoring and close-out visits, support subject recruitment plans, and ensure accurate documentation and training at assigned sites, while traveling as required.

Formación

• Bachelor's degree in health care or other scientific discipline or equivalent education.
• At least 4 years of on-site monitoring experience.
• Advanced in English.
• In-depth knowledge of GCP, ICH guidelines, and regulatory requirements.
• Strong organizational and time management skills.
• Excellent communication and interpersonal skills.
• Ability to work independently and as part of a team.
• Proficiency in CTMS and EDC systems.
• Willingness to travel as required.

Responsabilidades

• Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation
• Supporting the development of a subject recruitment plan
• Establishing regular communication plus administering protocol and study training to sites
• Evaluating site practices for quality and escalating issues as needed
• Managing progress by tracking regulatory submissions, recruitment, CRF completion, and data queries
• Collaborating with diverse colleagues and customers; knowledge of applicable regulatory requirements

Conocimientos

Site monitoring

English proficiency

Regulatory knowledge

Communication skills

Time management

Teamwork

CTMS

EDC

Travel readiness

Educación

Bachelor's degree in health care or scientific discipline

Herramientas

CTMS

EDC

Descripción del empleo

IQVIA in Buenos Aires, Argentina, is seeking a Senior Clinical Research Associate to oversee site monitoring, data integrity, and regulatory compliance across multicenter clinical trials.

You will perform site selection, initiation, monitoring and close-out visits, support subject recruitment plans, and ensure accurate documentation and training at assigned sites, while traveling as required.