Performs on-site or remote Pre-Study, Initiation, Interim, and Close-Out monitoring visit
Identifies the investigators and verifies that the investigator has adequate qualifications
Trains investigational site staff as necessary
When applicable, supports preparation of regulatory and / or EC submissions
Participates in mentoring/training of new staff as well as performing co-monitoring visits, to

🎯 Requirements

College/University degree in Life Sciences or an equivalent combination of education, training
Extensive on-site monitoring experience in phase 2/3 trials, ideally with experience of complex
Full working proficiency in English
Ability to plan, multitask and work in a dynamic team environment
Communication, collaboration, and problem-solving skills
Ability to travel nationally

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