Scientific Editor - (Boston, MA)

Work directly with scientists within Early Development and Research and Clinical/ Regulatory Operations and Regulatory Affairs departments on various nonclinical regulatory documents (e.g. Investigator Brochures, Nonclinical Study Reports, Annual Reports, CTAs, INDs, and NDAs, specialized Regulatory documents) as well as nonclinical publications and study reports. This position can assume lead scientific writing responsibility on these projects if needed, utilizing both regulatory and publication documentation ability. This position can also lead writing assignments on other programs in early development. Writes nonclinical study report drafts from templates, nonclinical portions of investigators brochures, annual reports, INDs, IMPDs, and NDAs and other regulatory documents in conjunction with the scientists and project team with minimal supervision.