Job Description

National Travel Required.

Performs on-site or remote Pre-Study, Initiation, Interim, and Close-Out monitoring visit activities to ensure that facilities and staff at the investigational site continue to be adequate for the conduct of the study.

Identifies the investigators and verifies that the investigator has adequate qualifications, resources, facilities, equipment, and staff to conduct the clinical study throughout the study period.

Trains investigational site staff as necessary.

When applicable, supports preparation of regulatory and/or EC submissions.

Qualifications

• College/University degree in Life Sciences or an equivalent combination of education, training & experience
• Extensive on-site monitoring experience in phase 2/3 trials, ideally with experience of complex trials such as oncology / rare
• Full working proficiency in English
• Ability to plan, multitask and w...