Senior Clinical Research Associate (Sr CRA 3)

About the role

IQVIA Biotech is seeking an experienced Senior Clinical Research Associate (Sr CRA 3) to join its Clinical Monitoring team in Argentina. You will independently manage and monitor clinical trial sites, ensuring compliance with protocols, GCP, ICH guidelines, and regulatory requirements.

Key responsibilities

• Conduct site qualification, initiation, routine monitoring, and closeout visits.
• Support patient recruitment and retention, provide protocol training, and resolve quality or compliance issues.
• Track study milestones, review source documentation, and manage data query resolution.
• Maintain regulatory and essential documents and produce timely monitoring reports.
• Collaborate with cross‑functional teams and mentor junior CRAs through co‑monitoring and training.

Required profile

• Bachelor’s degree in a scientific, healthcare or related discipline (or equivalent experience).
• Minimum 4 years of on‑site clinical monitoring experience.
• Strong knowledge of GCP, ICH guidelines, FDA regulations and clinical trial processes.
• Excellent organizational, communication and problem‑solving abilities.

Required skills

• Proficiency with Microsoft Office applications.
• Experience using clinical trial management systems.