Senior Medical Writer(US)

GeneDx (Nasdaq: WGS) delivers personalized and actionable health insights to inform diagnosis, direct treatment, and improve drug discovery. The company is uniquely positioned to accelerate the use of genomic and large\-scale clinical information to enable precision medicine as the standard of care. GeneDx is at the forefront of transforming healthcare through its industry\-leading exome and genome testing and interpretation services, fueled by the world's largest, rare disease data sets. For more information, please visit www.genedx.com. **Summary** The Lead Scientific Writer will be a highly skilled and detail\-oriented professional, joining our dynamic team in medical affairs. This individual will have a strong background in medical writing including peer\-reviewed publications, particularly in genetics and genomics. This role involves creating clear, accurate, and relevant publications for a variety of healthcare professionals. This individual will work cross functionally with both internal stakeholders and external collaborators to drive the dissemination of research study findings through peer\-reviewed publications. **Job Responsibilities** * Develop and write high\-quality scientific and medical content, including congress abstracts, posters, presentations and peer\-reviewed original research articles and clinical studies. * Coordinate manuscript submissions, draft reviewer response documents, and revise and resubmit manuscripts and relevant supplementary materials to peer\-reviewed journals. * Collaborate with cross\-functional teams on manuscripts, including researchers, clinicians, and regulatory affairs, to ensure accuracy of scientific content and compliance with industry standards. * Conduct thorough literature reviews and stay updated on the latest advancements in genetics and genomics. * Translate complex scientific information into clear and accessible language for diverse audiences, including collaborators and management. * Ensure all written materials adhere to company guidelines, regulatory requirements, and best practices in medical writing (e.g. ICMJE and GPP best\-practice guidelines). * Participate in the development and review of standard operating procedures (SOPs) related to medical writing and publication development activities. * Coordinate the Medical, Legal, and Regulatory review process for publications (publication review committee; PRC) in JIRA. **People Manager** * No **Education, Experience, and Skills** * Master's degree in genetics, molecular biology, or a related field. * 5\+ years of professional medical writing experience in an industry setting, preferably in the IVD and 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 ve