Analista de Pesquisa Clínica Jr

Manage investigator site relationships to ensure effective delivery of clinical trials, including enrollment and database release. Conduct remote and onsite monitoring of clinical trial activities, ensuring compliance with protocols and regulations. Identify and resolve investigator site issues, and prepare close-out activities within required timelines.

Bachelor’s degree in life sciences or equivalent. Minimum 1-year relevant experience in clinical research site monitoring and management. Knowledge of clinical trial methodologies, ICH/GCP, and local regulations. Must be fluent in English and the native language of the country.

Significant travel (60-80%) within the area is required, including some international travel and weekend travel.