• 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.