GeneDx

Senior Medical Writer

GeneDx

full-time

Posted on:

Location Type: Remote

Location: United States

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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