The Senior Medical Writer is responsible for writing, editing, and/or reviewing clinical documents including, but not limited to, clinical study reports, investigator’s brochures, protocols, and integrated regulatory summary documents. This...

•Review, provide comments on, and prepare documents for submission to FDA and international regulatory authorities including protocols, investigator brochures, nonclinical and CMC amendments, and other regulatory documents. •Lead teams on the...

This person will be a member of the Clinical Contracts and Outsourcing Team. This person will assist FibroGen team members in the drafting, negotiation and administration of non-disclosure, vendor services, and other agreements. This position will...

FibroGen seeks a highly experienced Senior CRA with in-depth knowledge of Phase I through III Clinical Trials. The successful candidate will, working closely with the Clinical Program Manager, be responsible for the planning, implementation,...