GeneDx
genetics
PrincipalMedicalWriter
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“Principal Medical Writer at GeneDx. Skills: scientific publications portfolio development, scientific writing, publication planning, medical writing, cross-functional collaboration. development, execution, and operational oversight of the company’s scientific publications portfolio. lead the development of peer-reviewed manuscripts, abstracts, posters, and other scientific communications”
What You'll Achieve.
producing high-quality work; enhancing patient care; providing clear, accurate, and meaningful answers; delivering more diagnostic findings to individuals; helping patients get diagnosed earlier; make a tangible impact each day
Industry & Context.
solving complex problems with independence
fully remote position, work from a home office or other suitable remote location with reliable high-speed internet access, sedentary role requiring prolonged periods of sitting while working at a computer, Sitting for extended periods (up to 8 hours per day), Repetitive use of hands and fingers for typing and mouse operation, Visual acuity for reading computer screens and documents, Occasional lifting of up to 10 pounds (office supplies, equipment)
What They're Looking For.
Must Have
3-5 years of professional medical writing experience in an industry setting, understanding of scientific research methodologies, understanding of research consents, understanding of regulatory requirements, publication record with over 10 publications in the field of medical genetics and genetic testing, Experience in solving complex problems with independence, Ability to work both in a team environment and independently, Ability to manage multiple projects simultaneously, Attention to detail and commitment to producing high-quality work
Nice to Have
preferably in the genetic testing space
What You'll Do.
and operational oversight of the company’s scientific publications portfolio
lead the development of peer-reviewed manuscripts
and other scientific communications
Develop and write high-quality scientific and medical content
Translate complex scientific data into clear
compelling communications
Support end-to-end publication processes
Oversee and manage the publication planning and execution process
Ensure all publications adhere to company guidelines
regulatory requirements
Oversee publication review and approval process
and implement SOPs and best practices for publication development and medical writing
How You'll Work.
Team & Collaboration
Collaborate with cross-functional teams on publication development, including internal teams and external collaborators; work both in a team environment and independently; support one another
Communication Scope
Excellent written and verbal communication skills; Ability to communicate effectively via phone and video calls
Process & Methodology
publication planning, timeline management, managing multiple projects simultaneously
Full Job Description
Summary The Principal Medical Writer is a hands-on leadership role responsible for the development, execution, and operational oversight of the company’s scientific publications portfolio. This individual will lead the development of peer-reviewed manuscripts, abstracts, posters, and other scientific communications that support clinical, research, and commercial objectives. The role combines leadership in publication planning along with scientific writing and cross-functional collaboration within the clinical genomics environment. Job Responsibilities Develop and write high-quality scientific and medical content, including congress abstracts, posters, presentations, and peer-reviewed original research articles. Translate complex scientific data into clear, compelling communications tailored to diverse audiences. Collaborate with cross-functional teams on publication development, including internal teams and external collaborators. Support end-to-end publication processes, including planning, drafting, submission, peer review responses, and resubmissions. Oversee and manage the publication planning and execution process, including alignment with evidence generation strategies, resourcing, and timeline management. Ensure all publications adhere to company guidelines, regulatory requirements, and best practices in medical writing (e. g. ICMJE and GPP best-practice guidelines). Oversee publication review and approval process, including tracking and documentation systems. Develop, refine, and implement SOPs and best practices for publication development and medical writing. Education, Experience, and Skills Advanced degree (MS, PhD, MD or similar) in genetics, molecular biology, or a related field. 3-5 years of professional medical writing experience in an industry setting, preferably in the genetic testing space. Strong understanding of scientific research methodologies, research consents, and regulatory requirements. Strong publication record with over 10 publications
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