Especialista em Pesquisa Clínica

Manage investigator site relationships to ensure effective delivery of clinical trials. Conduct onsite and remote monitoring for study site initiation, routine monitoring, and closure activities. Resolve protocol-related issues for assigned investigator sites and ensure compliance with Good Clinical Practices.

Medical background or equivalent. Minimum 3 years of relevant experience in clinical research site monitoring, preferably 2 years in Oncology. Must be fluent in English and the native language of the country they will work in.

Significant travel (60-80%) within the area is required. May require some international travel and some weekend travel. Valid passport required.