Independently conduct and document onsite and remote activities, including site monitoring and
Collaborate with site staff to review and ensure that the data reported in the applicable study
Monitor, resolve and/or facilitate resolution of data queries and escalate issues as appropriate
Coordinate the shipment of clinical supplies, including but not limited to, investigational
Ensure site staff is trained in all aspects of the study including but not limited to the protocol
Participate in routine study progress meetings, teleconferences, and Investigator's meetings

🎯 Requirements

4 - 6 years of related experience
7 – 9 years of related experience (preferred)
(Honors) Bachelor’s degree
Master’s degree (preferred)
Fluent in written and verbal English
Health Sciences, Life Sciences, Pharmacy, or Nursing degree preferred, or Sr.CRA and/or ACRP

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