Responsible for the site management, site monitoring and close-out of assigned clinical trials investigator sites
Oversee the proper conduct of clinical trials in accordance with the Study Monitoring Plan (SMP) and applicable laws
Manage assigned operational aspects for implementation of clinical trial activities
Serve as the primary point of contact for assigned investigator sites
Support the study clinician in ensuring patient safety, eligibility and providing clinical guidance

3+ years of experience in clinical research site monitoring (preferably 2 years in Oncology)
Extensive knowledge of clinical trial methodologies, ICH/GCP, FDA and local country regulations
Must be fluent in English and in the native language(s) of the country they will work in
Valid driver’s license and passport required

Senior Clinical Research Associate – FSP

Key skills