- ThermoFisher Scientific (Greenville, NC)
- **Work Schedule** Standard (Mon-Fri) **Environmental Conditions** Office **Job Description** ** Principal Medical Writer ** At Thermo Fisher Scientific, you'll ... team is growing, and we are looking for a Principal Medical Writer . This role...research. Your expertise will enable us to deliver flawless Regulatory Medical Writing documents, such as protocols,… more
- Parexel (Dover, DE)
- **Parexel FSP is looking for a Principal Medical Writer ! This is a remote role anywhere in the United States or Canada.** Job Purpose: The Medical ... products and projects. This individual will work with the lead and/or program medical writer and independently to develop messages and write, substantively… 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 ... serves to generate timely, high quality, cost effective and regulatory compliant documents. Our mission is to synergize and...**About You** **Core Experience** : + Six+ years as medical writer or equivalent specialist role +… more
- J&J Family of Companies (Spring House, PA)
- …Johnson & Johnson Innovative Medicine R&D is recruiting for a Senior Principal Scientist, Nonclinical Submissions Writer . This position is a hybrid ... be located in Spring House, PA or San Diego, CA. The Senior Principal Scientist, Nonclinical Submissions Writer , within the Preclinical Sciences and… more
- ThermoFisher Scientific (Greenville, NC)
- …Schedule** Standard (Mon-Fri) **Environmental Conditions** Office **Job Description** **FSP Senior** ** Regulatory ** ** Medical Writer (** **Remote;** **US** ... candidates based in the US! As a remote-based Senior Medical Writer within the FSP team, you...possess the versatility to author both clinical and preclinical regulatory documents, with therapeutic area expertise in infectious diseases… more
- IQVIA (Durham, NC)
- **Job Overview:** As a Lead Medical Writer on most types of writing projects. You will prepare assigned documents in accordance with IQVIA Standard Operating ... junior staff, and to customers when appropriate. Keep abreast of current medical and/or technical writing/ regulatory knowledge, including Good Clinical Practice… more
- Roche (Branchburg, NJ)
- …for generations to come. Join Roche, where every voice matters. **The Position** As the Principal Technical Writer , you will operate at the highest level in the ... technical writing series, providing strategic leadership and definitive regulatory guidance for all documentation projects. Your responsibilities will include… more
- Houston Methodist (Houston, TX)
- At Houston Methodist, the Senior Scientific Writer is responsible for functioning as the mentor for junior staff with an extensive knowledge of both medical and ... present data considering scientific communications best practices. + Works with Principal Investigator(s) to develop, present, and bring to final submission high… more
- IQVIA (Durham, NC)
- …teams that include Project Manager, CRA, Data Manager, Biostatistician, Programmer, and/or Medical Writer . + Maintain awareness of overall developments in the ... **Job Level:** Senior/ Principal Pharmacometrician, FSP **Location:** Home-based in the US...sections of dossiers for product registration and communicate with regulatory agencies. + Assess pharmacometric requirements for and ensure… more
- Microsoft Corporation (Redmond, WA)
- …critical priorities for our customers in a world awash in digital threats, regulatory scrutiny, and estate complexity. Microsoft Security aspires to make the world a ... be an opportunity for you. The security team seeks a motivated, experienced Principal Technical Security Program Manager to join our benchmarking team. We are… more