Senior Medical Writer - Remote
3 days ago

Job description
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
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 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.
Preferred:
- Advanced degree (PhD, MD, or equivalent) in genetics, molecular biology, or a related field.
- Familiarity with genetic testing technologies and their clinical applications.
Certificates, Licenses, Registrations
- Certified Medical Publication Professional (CMPP) or equivalent
- Membership in professional medical writing organizations (e.g., AMWA, EMWA).
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 in collaboration with your leader and may be adjusted to align with evolving business needs.
Physical Demands
This is a sedentary role requiring prolonged periods of sitting while working at a computer. Physical demands include:
- Sitting for extended periods (up to 8 hours per day)
- Repetitive use of hands and fingers for typing and mouse operation
- Visual acuity for reading computer screens and documents
- Ability to communicate effectively via phone and video calls
- Occasional lifting of up to 10 pounds (office supplies, equipment)
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this position.
Acknowledgements
The above job description is not intended to be an all-inclusive list of duties and standards of the position. Incumbents will follow any other instructions and perform any other related duties, as assigned by their supervisor.
#LI-REMOTE
Pay Transparency, Budgeted Range $120,000—$130,000 USD~
Science - Minded, Patient - Focused.
At GeneDx, we create, follow, and are informed by cutting-edge science. With over 20 years of expertise in diagnosing rare disorders and diseases, and pioneering work in the identification of new disease-causing genes, our commitment to genetic disease detection, discovery, and diagnosis is based on sound science and is focused on enhancing patient care.
Experts in what matters most.
With hundreds of genetic counselors, MD/PhD scientists, and clinical and molecular genomics specialists on staff, we are the industry's genetic testing experts and proud of it. We share the same goal as healthcare providers, patients, and families: to provide clear, accurate, and meaningful answers we all can trust.
SEQUENCING HAS THE POWER TO SOLVE DIAGNOSTIC CHALLENGES.
From sequencing to reporting and beyond, our technical and clinical experts are providing guidance every step of the way:
TECHNICAL EXPERTISE
- High-quality testing: Our laboratory is CLIA certified and CAP accredited and most of our tests are also New York State approved.
- Advanced detection: By interrogating genes for complex variants, we can identify the underlying causes of conditions that may otherwise be missed.
CLINICAL EXPERTISE
- Thorough analysis: We classify variants according to our custom adaptation of the most recent guidelines. We then leverage our rich internal database for additional interpretation evidence.
- Customized care: Our experts review all test results and write reports in a clear, concise, and personalized way. We also include information for research studies in specific clinical situations.
- Impactful discovery: Our researchers continue working to find answers even after testing is complete. Through both internal research efforts and global collaborations, we have identified and published hundreds of new disease-gene relationships and developed novel tools for genomic data analysis. These efforts ultimately deliver more diagnostic findings to individuals.
Learn more About Us here.
Our Culture
At GeneDx, we are dedicated to cultivating an environment where creativity and innovation thrive. We believe in the power of community and collaboration, where diverse perspectives are embraced, and every voice contributes to our shared success. Our team is a vibrant mix of professionals who challenge and support each other in equal measure, fostering growth both personally and professionally. When you join us, you're not just taking on a job—you're joining a movement. A movement that champions curiosity, embraces change, and believes in making an impact, one patient at a time. Cultural principles we live by:
- Be bold in our vision & brave in our execution.
- Communicate directly, with empathy.
- Do what we say we're going to do.
- Be adaptable to change.
- Operate with a bias for action.
Benefits include:
- Paid Time Off (PTO)
- Health, Dental, Vision and Life insurance
- 401k Retirement Savings Plan
- Employee Discounts
- Voluntary benefits
GeneDx is an Equal Opportunity Employer.
All privacy policy information can be found here.
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