Reporting to a Clinical Program Manager (CPM), the successful incumbent will assist with operational activities for two phase two trials in China. The therapeutic area is anemia.
Duties include, but are not limited to:
May monitor study sites for data collection, source data verification, review of regulatory documents/files and drug accountability
May review and edit documents including protocols, informed consents, case report forms, monitoring plans, edit specifications, abstracts, ...
FibroGen, Inc. - 4 months ago
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