Medical Program Clinical Specialist/ Clinical Associates

Job Description:
The MPCS will support the MRL clinical monitors who oversee
the conduct of Phase II / III clinical trails, including assisting in
medical data review, the ordering of clinical supplies, tabulation of
clinical data (excel spreadsheets) and writing of clinical summaries. With
the exception of actions requiring medical judgment, the incumbents
provide support to assure that program objectives are achieved.
Requirements: bachelor's degree in biological, chemical nursing or
pharmaceutical sciences and at least three years of experience in clinical
research or equivalent experience. Direct clinical experience or
experience conducting clinical research in the pharmaceutical industry.
Good computer skills, able to multi-task and effective team communication
abilities.
**** EXTENSIVE SCIENTIFIC / MEDICAL WRITING EXPERIENCE NEEDED ***
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Job Experience:
call for details, Scientific Writing and Medical Writing

Searchable Keywords: call for details, Scientific Writing and Medical Writing / gj-mo