Merck seeks a Clinical Research Manager to lead operational execution of clinical studies in Argentina from initiation through closeout. The role coordinates investigators, sites, vendors, and internal teams to ensure compliance with timelines, quality standards, protocols, GCP, and regulatory requirements while managing risks and driving effective study delivery.
Responsibilities
Lead operational execution of assigned clinical studies from startup through closeout
Ensure study activities comply with timelines, quality standards, protocols, GCP, and regulatory requirements
Coordinate with investigators, research sites, CRAs, vendors, and internal study teams
Monitor study performance using clinical systems, dashboards, and data-driven metrics
Identify and mitigate operational, regulatory, quality,



financial, and timeline risks
Requirements
Bachelor's degree in Life Sciences, Health Sciences, or related field
More than 6 years of relevant clinical research experience
Previous Clinical Research Associate experience with at least 3 years of clinical monitoring
Advanced English proficiency for general cross-functional communication
Strong knowledge of clinical research operations, GCP, and local regulations
Demonstrated experience collaborating with investigators, sites, vendors, and cross-functional teams
Oncology experience preferred

📌 Clinical Research Manager (Crm) (Buenos Aires)
🏢 Merck
📍 Buenos Aires