Sanofi

Associate Director, Medical Value and Outcomes (Mid-Atlantic) The Medical Value & Outcomes team member serves as the medical scientific lead for population-based healthcare decision makers to facilitate scientific exchange on disease state management and the value of Sanofi Genzyme products, to provide insights to internal teams on key evidence gaps relevant to healthcare decision-makers, and to identify/facilitate research, education, and other collaborations per applicable SOPs. This position represents the MS and Immunology franchises serving as the MVO lead for assigned strategic regional accounts. The position supports the strategic and cross functional alignment within the organization in order to achieve the medical mission of safe and appropriate use of Sanofi Genzyme therapies. The MVO assists in the development of Integrated Medical Plans through collaboration with Medical Communications and Publications, Medical Science Liaisons, and Health Outcomes personnel for...

Job Title: Associate Director, Medical Value and Outcomes (Mid-Atlantic) Location : Remote/Field About the Job The Medical Value & Outcomes team member serves as the medical scientific lead for population-based healthcare decision makers to facilitate scientific exchange on disease state management and the value of Sanofi Genzyme products, to provide insights to internal teams on key evidence gaps relevant to healthcare decision-makers, and to identify/facilitate research, education, and other collaborations per applicable SOPs. This position represents the MS and Immunology franchises serving as the MVO lead for assigned strategic regional accounts. The position supports the strategic and cross functional alignment within the organization in order to achieve the medical mission of safe and appropriate use of Sanofi Genzyme therapies. The MVO assists in the development of Integrated Medical Plans through collaboration with Medical Communications and Publications,...

Associate Director, Medical Value and Outcomes (Mid-Atlantic) The Medical Value & Outcomes team member serves as the medical scientific lead for population-based healthcare decision makers to facilitate scientific exchange on disease state management and the value of Sanofi Genzyme products, to provide insights to internal teams on key evidence gaps relevant to healthcare decision-makers, and to identify/facilitate research, education, and other collaborations per applicable SOPs. This position represents the MS and Immunology franchises serving as the MVO lead for assigned strategic regional accounts. The position supports the strategic and cross functional alignment within the organization in order to achieve the medical mission of safe and appropriate use of Sanofi Genzyme therapies. The MVO assists in the development of Integrated Medical Plans through collaboration with Medical Communications and Publications, Medical Science Liaisons, and Health Outcomes personnel for...

A leading pharmaceutical company is seeking a Principal Medical Writer Associate Director. This remote position involves creating regulatory-compliant clinical documents, leading digital innovations, and managing project initiatives. Candidates should have over six years of experience in medical writing, strong regulatory expertise, and the ability to work within global teams. Competitive compensation and a comprehensive benefits package are offered. #J-18808-Ljbffr

**Job Title:** Principal Medical Writer Associate Director**Location**: USA, Remote. Proximity to Cambridge/Boston, MA or Morristown, NJ is highly desirable for attending occasional team meetings**About the Job**Global Medical writing and Document management serves to generate timely, high quality, cost effective and regulatory compliant documents. Our mission is to synergize and harness evolving technologies pushing the edge of regulatory writing.**Main Responsibilities:****Document Development*** Create high-quality regulatory-compliant clinical documents supporting product life cycle* Ensure timely delivery while maintaining compliance with standards**Innovation*** Lead implementation of new digital technologies and AI solutions* Drive process improvements for efficiency gains**Regulatory Expertise*** Prepare registration dossiers and Health Authority responses* Monitor and implement regulatory documentation requirements**Project Management*** Lead cross-functional initiatives...