Responsible for ensuring study is compliance with local and federal laws and regulations
Consents subject according to FDA requirements
Recruits and screens potential study participants and performs intake assessments
Creates and/or maintains all documents and records related to the study
Extracts and inputs data as required into electronic systems
Acts as a point of reference for study participants by answering questions and keeping them informed on the study progress
Manages the inventory of equipment and supplies related to the study and orders more as needed
Attends meetings, events and seminars in order to promote the study
Is a Liaison between study site, sponsors, cro, labs, ect
Collects specimens (phlebotomy a plus), may process in a lab, and ship specimens (IATA familiarity a plus)
Creates reports on each study, including notes on protocols, workload, data collection, and more
May need to travel between work sites to meet with trail participants
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