The Clinical Research Associate coordinates and monitors clinical study sites to ensure compliance with GCP requirements, study protocols, and regulatory standards. They also manage study documentation, track adverse events, and facilitate data entry and query resolution to support project timelines.
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.
