Sr. Medical Writer - Boston - (Boston, MA)

The Senior Medical Writer is responsible for preparing clinical study documents and sections of regulatory submissions. The Senior Medical Writing Scientist may assist other Medical Writing staff to prepare more complex documents and may assist with developing documents produced by other departments. The Senior Medical Writing Scientist contributes scientific knowledge and issue solving abilities to the preparation of clinical regulatory documentation. Works under minimal supervision. ESSENTIAL RESPONSIBILITIES: - Broad understanding of drug development, clinical research, study designs, biostatistics, pharmacology, regulatory qualifications, and medical terminology. - Background writing and editing clinical regulatory documents - Serve as the lead Medical Writing Scientist for moderately complex clinical studies - Expertise to manage project teams, form productive working relationships, and work through conflicts - Perform other duties as assigned The Successful applicant will have: