Argenta

Lead the execution of the US Clinical strategy and business plan while fostering a high-performance culture. Manage client expectations and oversee clinical personnel to ensure project compliance and high-quality data delivery.

Facilitates regulatory and drug development requirements for external clients and internal projects within the animal health sector. Provides expert regulatory advice and represents the company in industry associations to identify new consulting opportunities.

The role involves coordinating and monitoring GCP clinical trials at study sites to ensure protocol compliance and data integrity. The CRA serves as the primary liaison between the organization and study site personnel to resolve data queries and track adverse events.