Clinical Trials GMP/GDP Compliance Specialist

Trf (Transfarmaco Sa); Buenos Aires; Presencial; ARS 105.910.000 - 181.560.000; Jornada completa

Descripción de la vacante

IQVIA is seeking a Clinical Trial Coordinator II to direct site activation and maintenance activities across multiple studies, ensuring regulatory compliance and timely delivery. You will support eTMF reviews, CTMS updates, and communications with regions and sites.

Join a global leader in clinical research services, delivering high-quality trial execution and regulatory support to enable successful study initiation and continued oversight.

Formación

• Bachelor's degree preferred.
• 2+ years of relevant clinical trial coordination experience.
• Strong understanding of regulatory requirements for clinical studies.

Responsabilidades

• Coordinate site activation and maintenance activities for assigned trials per the project plan.
• Perform (e)TMF reviews, document findings, and ensure timely document distribution.
• Maintain CTMS data accuracy and provide regular status updates to project leads.
• Support regulatory submissions and keep stakeholders informed of risks and mitigations.

Conocimientos

Regulatory strategy

Project management

CTMS proficiency

eTMF documentation

Educación

Bachelor's degree

Herramientas

CTMS

eTMF systems

Regulatory databases

Descripción del empleo

IQVIA is seeking a Clinical Trial Coordinator II to direct site activation and maintenance activities across multiple studies, ensuring regulatory compliance and timely delivery. You will support eTMF reviews, CTMS updates, and communications with regions and sites.

Join a global leader in clinical research services, delivering high-quality trial execution and regulatory support to enable successful study initiation and continued oversight.