Medical Writer I - Drug Safety & Disposition

Medical Writer I - Drug Safety & Disposition Job Description:Company Information:Breakthrough Careers!A career at Millennium comes with something no other company can offer: a community of people with diverse talents and backgrounds, all dedicated to the discovery and development of therapies that can change the world - one patient at a time. Our casual but focused environment fosters the free exchange of ideas, encourages collaborative research, and sparks discovery of innovative solutions in science and business. At Millennium, we're big on results, not formality.Position Summary:Medical Writers are critical to the success of the Nonclinical Writing group and are primarily responsible for editing nonclinical study reports and submission sections, as well as timeline management related to those documents.Duties and Responsibilities:Edit and revise nonclinical study reports, protocols and accompanying sections of global regulatory submissions (IND, CTA, IB, NDA, etc). Ensure that scientific content is clear, accurate, well-organized, and consistent within individual documents and across filings. Manage review and approval processes to ensure integrity of filings. Serve as nonclinical writing representative on cross-functional teams. Consistently meet tight timelines.Qualifications:Preferred Qualifications: BS/BA or higher with 3 or more years experience as a medical/science writer and/or editor in a pharmaceutical, communications, or journalistic setting is preferred. Candidate should have a keen eye for detail and ensure that complex medical or scientific information is presented in a clear, readable and accurate fashion; candidate should also be flexible, self-starter, and able to work with minimal supervision to achieve objectives in a timely manner; should possess strong interpersonal and organizational skills. Working with the nonclinical authors to address questions and comments from various functional areas (Regulatory, Clinical, etc.) on nonclinical submission questions; must be comfortable taking initiative and working with scientists to ensure that scientific content is accurate, concise, and clear; and must be able to juggle numerous projects at once, prioritize competing needs, and work well under deadline pressure. Familiarity with AMA Manual of Style, Microsoft Word, Microsoft Project, and Electronic Document Management systems are a plus.Basic Qualifications: Min of 3 years as a medical or science writer/editor in a pharma/biotch, medical or closely related and regulated industry. A background, training or degree in a science/medical related field.Click here to immediately applyWant to learn more about us? Years of Experience Required: 3-5 YearsExpected Travel Time: None Searchable Keywords: SAS / gj-moExpected Travel Time: None Company: Millennium Pharmaceuticals, Inc. Contact: Recruiter Email: Apply by Email Address: 02454 Reference Code: 14467.26412.5440BR Company: Millennium Pharmaceuticals, Inc. Status: Full Time, Employee Job Category: Biotech/R&D/Science