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Principal Medical Writer

GeneDx

4h ago

0$160k - $170kWritingRemote, USjobspy_indeed
remoteindeed

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 in the field of medical genetics and genetic testing. * Experience in solving complex problems with independence. * Excellent written and verbal communication skills. * 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. * Proficiency in data visualization and figure design to display data in an easily digestible format. * Proficiency in Microsoft Office Suite, reference management, and data visualization software. **Work Environment** * This is a fully remote position. The employee will work from a home office or other suitable remote location with reliable high\-speed internet access. Work is performed in a climate\-controlled environment using standard office equipment including computer, phone, and video conferencing tools. Your standard work schedule and hours will be established i