Global Clinical Research Associate - Hybrid Site Manager

Merck Gruppe - MSD Sharp & Dohme; Argentina; Hybrid; ARS 1,200,000 - 2,000,000; Full time

Job summary

Merck Sharp & Dohme is seeking a Clinical Research Associate for site management in Argentina, focusing on monitoring activities across trial phases and ensuring compliance with ICH‑GCP and local regulations. The role involves remote and on-site oversight, site qualification, and close collaboration with Sponsors and site staff.

You will manage CTMS/eTMF documentation, participate in audits, and support teams with best practices in monitoring processes. Hybrid work arrangements are offered.

Qualifications

• Minimum 2 years direct site management (monitoring) experience in bio/pharma/CRO.
• Fluent in English (verbal and written).
• BA/BS with strong emphasis in science and/or biology.

Responsibilities

• Develops strong site relationships across all trial phases.
• Performs site management/monitoring activities in compliance with ICH-GCP and local laws.
• Coordinates with sponsor roles to achieve Site Ready; supports site selection and validation.
• Performs remote and on-site monitoring to ensure data integrity and subject safety.
• Maintains documentation in CTMS/eTMF and other systems per timelines.
• Contributes to CRA team knowledge as SME and mentor.

Skills

Fluent English

Site management

Monitoring

Data analysis

MS Office

Education

BA/BS in science or biology

Tools

CTMS

eTMF

Job description

Merck Sharp & Dohme is seeking a Clinical Research Associate for site management in Argentina, focusing on monitoring activities across trial phases and ensuring compliance with ICH‑GCP and local regulations. The role involves remote and on-site oversight, site qualification, and close collaboration with Sponsors and site staff.

You will manage CTMS/eTMF documentation, participate in audits, and support teams with best practices in monitoring processes. Hybrid work arrangements are offered.