- Sanofi Group (Morristown, NJ)
- …clinical documents and regulatory dossiers and has demonstrated leadership skills as submission lead . As an integral part of the clinical team, the position ... clinical studies not covered by the standards and technical expertise gained with advanced technologies. + Review ...equivalent, or presenting relevant specialist qualifications. + Experience as Lead Project MW on multiple types of clinical… more
- Stryker (Portage, MI)
- As the Technical Writer for Stryker's Acute Care team, you will play a critical role in delivering clear, accurate, and user-friendly documentation for both ... process + Develop working relationship with Regulatory Affairs, Quality Engineering, Technical Support, R&D, Clinical Affairs, Compliance Engineering, and… more
- United Therapeutics (Research Triangle Park, NC)
- …interpretations are accurately and clearly reflected in relevant documents. + Serve as lead author for complex clinical and regulatory documents including ... detail-oriented with deep expertise in regulatory submissions and writing, including clinical study reports, clinical study protocols, and investigator's… more
- CVS Health (Woonsocket, RI)
- …**Description:** Reporting to the Core Creative Manager for Experience Design, the Sr. Writer will lead the writing for various projects and initiatives within ... and grammar. This person will have the ability to lead and generate ideas and themes, write concise descriptions...Qualifications:** + Minimum 5 years of working as a writer with an additional 2 years of experience in… more
- IQVIA (Durham, NC)
- …of sources in a clear and concise manner. + Significant experience as a lead writer in preparing CSRs and protocols, with consistently positive feedback from ... + Doit avoir une bonne maitrise des outils informatiques. **Job Overview:** Acts as Lead Medical Writer on most types of writing projects. Prepares assigned… more
- Sanofi Group (Morristown, NJ)
- **Job Title:** Principal Medical Writer Associate Director **Location** : USA, Remote. Proximity to Cambridge/Boston, MA or Morristown, NJ is highly desirable for ... started? **Main Responsibilities:** **Document Development** + Create high-quality regulatory-compliant clinical documents supporting product life cycle + Ensure timely… more
- New York Genome Center (New York, NY)
- …multi-PI and research center grants. Key Responsibilities + Takes a lead role in preparation and project management of individual and multi-investigator ... submission. + Edits manuscripts, fellowship applications, research progress reports, clinical research protocols and other research communications materials. +… more
- University of Rochester (Rochester, NY)
- …time and meet required deadlines Required + Contribute individually and as a technical lead on the team that manages multiple business environments; interface ... + Tableau Desktop Associate Level 1, Level 2 Preferred + Workday Report Writer curriculum certificate Preferred + Epic Clinical Data Model and/or Epic… more
- Queen's Health System (Honolulu, HI)
- …for Decision Support & Analytics systems, as assigned. * Serves as the lead System Administrator for the Activity Based Costing system, overseeing the development ... performance improvement opportunities from cost analysis and collaborates with clinical /physician leadership toward exploration/implementation of improvement initiatives. * Provides… more