Sr. Consultant, Medical Writing, Pharmaceuticals

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Irfa******

  • United States 
  • Last Update: 22.08.2019 at 12:00

Job Type
Full Time
Start
ASAP
Duration
6 Month +
Place
Cambridge, Massachusetts
Country
United States

Description


Overview

This consultant will provide leadership and functional oversight for one or more clinical program. This person functions as a strong project manager and technical leader, with demonstrated scientific and customer-focused leadership skills. They will direct medical writers in the preparation of clinical regulatory documents, including clinical summaries/overviews for marketing applications (including global markets and emerging markets) and clinical trial applications (INDs/CTAs). Will also partner with R

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