Description
Scope of Services:Under the direction of the Director of the Medical Writing department, this position will be accountable for authoring technical clinical/regulatory documents (such as Clinical Study Reports [CSRs], Protocols, Protocol Amendments, Investigator Brochures [IBs], Briefing Documents, Safety related documents, etc.) that may require clinical interpretation of data and synthesis of clinical safety and efficacy information as needed. The individual will work an average of 20 hours per week onsite or remotely in a home office.
Deliverables:
Description of Milestones/Deliverables
Estimated Completion Date
Oprozomib protocols/protocol amendments
December 2014
Carfilzomib protocols/protocol amendment
December 2014
Other clinical documents as needed
December 2014
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