Lead Scientific Writer

Lead Scientific Writer 

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 Principal Medical 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.

Essential Duties and Responsibilities:

• Develop and write high-quality scientific and medical content, including peer-reviewed research articles and clinical studies. May also write high profile conference abstracts.
• Collaborate with cross-functional teams on manuscripts, including researchers, clinicians, and regulatory affairs, to ensure accuracy 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.
• Participate in the development and review of standard operating procedures (SOPs) related to medical writing activities.
• Coordinate Medical, Legal, Regulatory (MLR) reviews and manuscript submissions to journals.

Qualifications:

• Master’s degree in genetics, molecular biology, or a related field.
• 5+ years of experience in medical writing, preferably in the field of genetics or genomics.
• 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 designing figures to display data in an easily digestible format
• Proficiency in Microsoft Office Suite and reference management software.

Preferred:

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