Clinical Site Monitor & Project Coordinator

IQVIA; México; Sur place; MXN 500 000 - 800 000; Plein temps

Résumé du poste

IQVIA is seeking a Senior Clinical Research Associate to perform site monitoring and site management across protocols and therapeutic areas. The role requires managing visits, site communications, and training of clinical staff to ensure study quality and regulatory compliance.

The candidate should have 5+ years of on-site monitoring experience, at least 1 year as a Senior CRA, and strong English communication skills. Proficiency in Excel and PowerPoint is expected.

Qualifications

• Bachelor's Degree in scientific discipline or health care preferred.
• Requires 5+ years on-site monitoring experience, minimum 1 year as SR CRA.
• Strong knowledge of GCP/ICH guidelines.
• Excellent English communication and problem-solving skills.

Responsabilités

• Conduct site monitoring visits (selection, initiation, monitoring, close-out) per contract scope and regulatory requirements.
• Coordinate subject recruitment plans with sites to support project needs.
• Train and mentor clinical staff; conduct co-monitoring and training visits.
• Track regulatory submissions, recruitment, CRF completion, data queries, and TMF/ISF maintenance.
• Prepare visit reports and action plans; ensure site documents are filed appropriately.

Connaissances

On-site monitoring

Time management

Communication

Team collaboration

Formation

Bachelor's degree in science/health

Outils

Excel

PowerPoint

Description du poste

IQVIA is seeking a Senior Clinical Research Associate to perform site monitoring and site management across protocols and therapeutic areas. The role requires managing visits, site communications, and training of clinical staff to ensure study quality and regulatory compliance.

The candidate should have 5+ years of on-site monitoring experience, at least 1 year as a Senior CRA, and strong English communication skills. Proficiency in Excel and PowerPoint is expected.