
Senior Medical Writer
GeneDx
full-time
Posted on:
Location Type: Remote
Location: United States
Visit company websiteExplore more
Salary
💰 $120,000 - $130,000 per year
Job Level
About the role
- 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.
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.
- Advanced degree (PhD, MD, or equivalent) in genetics, molecular biology, or a related field preferred.
- Familiarity with genetic testing technologies and their clinical applications preferred.
- Certified Medical Publication Professional (CMPP) or equivalent preferred.
- Membership in professional medical writing organizations (e.g., AMWA, EMWA) preferred.
Benefits
- Paid Time Off (PTO)
- Health, Dental, Vision and Life insurance
- 401k Retirement Savings Plan
- Employee Discounts
- Voluntary benefits
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
medical writingscientific research methodologiesdata visualizationfigure designmanuscript submissionliterature reviewregulatory compliancepublication developmentclinical studiesgenetics
Soft Skills
excellent written communicationexcellent verbal communicationproblem-solvingattention to detailindependenceteam collaborationproject managementadaptabilitycommitment to qualityclear communication
Certifications
Certified Medical Publication Professional (CMPP)membership in AMWAmembership in EMWA