Senior Medical Writer(Canada)

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 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.   

Compensation: CAD$110,000 - CAD$130,000 (Eligible For Overtime)

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