Senior Medical Writer

GeneDx•Gaithersburg, MD

8d•$120,000 - $130,000•Remote

About The Position

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.

Requirements

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 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.

Nice To Haves

Advanced degree (PhD, MD, or equivalent) in genetics, molecular biology, or a related field.
Familiarity with genetic testing technologies and their clinical applications.
Certified Medical Publication Professional (CMPP) or equivalent
Membership in professional medical writing organizations (e.g., AMWA, EMWA).

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.