- Insmed Incorporated (NJ)
- …each other, and for the future of science, we're in. Are you?About the Role:The Principal Medical Writer is a REMOTE position, responsible for the ... writing point of contact for clinical study teams. May serve as the lead Medical Writer .Applies in-depth knowledge of medical writing and therapeutic… more
- Synterex (Boston, MA)
- Principal Medical Writer Synterex,...leading the planning and preparation of high-quality clinical and regulatory documents. The medical writer ... individual for our medical writing team. The principal medical writer will partner...with the requirements for preparation of key clinical and regulatory documents, including ICH and US/EMA regulatory … more
- Parexel (Madison, WI)
- **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
- Parexel (Bismarck, ND)
- **Job Summary:** The Principal Medical Writer is responsible for writing and overseeing the completion of a broad range of documents in support of company ... products and projects. This individual will work with the lead and/or program medical writer and independently to develop messages and write, substantively… more
- ThermoFisher Scientific (Wilmington, 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
- Sanofi Group (Morristown, NJ)
- **Job Title:** Associate Director- Principal Medical Writer **Location:** USA, Remote. Proximity to Cambridge/Boston, MA or Morristown, NJ is highly desirable ... be critical in helping our teams accelerate progress. The Principal Medical Writer is a...standards and procedures with the ultimate aim to gain regulatory approval of therapeutic indications. + Coordinate medical… 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
- IQVIA (Durham, NC)
- **Apercu du poste :** Agit a titre de redacteur medical principal pour la plupart des types de projets de redaction. Prepare les documents attribues conformement ... maitrise des outils informatiques. **Job Overview:** Acts as Lead Medical Writer on most types of writing...and to customers when appropriate. Keeps abreast of current medical and/or technical writing/ regulatory knowledge, including Good… 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
- 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
- AbbVie (North Chicago, IL)
- …peers, business stakeholders & management; + interpreting statistical data to prepare written medical and scientific reports for regulatory bodies; + clinical ... development, clinical research, study designs, & biostatistics to author clinical regulatory documents; + performing medical writing in the bio-pharmaceutical… more
- University of Miami (Miami, FL)
- …Miami/UHealth Department of SCCC has an exciting opportunity for a Full Time Hybrid Scientific Writer 2 to work at the UHealth medical campus in Miami, Fl. CORE ... SUMMARYThe Hybrid (1X a week or as necessary) Scientific Writer 2 collects and analyzes complex scientific data and...of the target audience. This job also assists the Principal Investigator (PI) with the development and/or completion of… more
- Houston Methodist (Houston, TX)
- At Houston Methodist, the Scientific Writer position is responsible for performing a variety of tasks including preparing laboratory and clinical studies and ... other communications venues. **PEOPLE ESSENTIAL FUNCTIONS** + Works with principal investigator, provides advice on grantsmanship, editorial support and standardized… more
- Houston Methodist (Houston, TX)
- The Houston Methodist Peak Brain & Pituitary Tumor Center seeks a scientific writer . The scientific writer will primarily be responsible for proofreading and ... present data considering scientific communications best practices. + Works with Principal Investigator(s) to develop, present, and bring to final submission high… more
- University of Miami (Miami, FL)
- …suggestion alternative language, as required. Communicates (telephone, email, meetings) with principal investigator and key senior leadership authors as necessary to ... Summarizes data from clinical studies for submission to appropriate governmental/ regulatory agencies. Edits all extramurally funded proposals for grammar,… more
- University of Utah (Salt Lake City, UT)
- …closely with numerous members of the clinical research team including the Principal Investigator (PI), Biostatistician, and Protocol Writer . This position will ... research. Must have a working knowledge of FDA , ICH , and other regulatory compliance; an understanding of medical terminology and technical writing experience.… more
