Sr Clinical Trial Manager (Sponsor dedicated) – BA, Argentina

Chiefly responsible for site management oversight, clinical monitoring, and central monitoring deliverables, ensuring protocol, GCP, and regulatory compliance while safeguarding patient safety and data integrity. Acts as the primary escalation point for investigator site staff and collaborates with cross‑functional teams to meet study milestones and maintain high quality clinical operations, with a focus on risk‑based monitoring and inspection readiness.

Job Responsibilities

• Provide site management oversight, including monitoring and central monitoring deliverables, focusing on patient safety, protocol/GCP/regulatory compliance, and data integrity.
• Oversee site interactions from activation through closeout, including patient recruitment and investigator payments.
• Identify critical data and process risks, complete Risk Assessment and Categorization Tool (RACT) and pr...