Develop and write high-quality scientific and medical content, including congress abstracts, posters, presentations, and peer-reviewed original research articles.
Translate complex scientific data into clear, compelling communications tailored to diverse audiences.
Collaborate with cross-functional teams on publication development, including internal teams and external collaborators.
Support end-to-end publication processes, including planning, drafting, submission, peer review responses, and resubmissions.
Oversee and manage the publication planning and execution process, including alignment with evidence generation strategies, resourcing, and timeline management.
Ensure all publications adhere to company guidelines, regulatory requirements, and best practices in medical writing (e.g. ICMJE and GPP best-practice guidelines).
Oversee publication review and approval process, including tracking and documentation systems.
Develop, refine, and implement SOPs and best practices for publication development and medical writing.

Advanced degree (MS, PhD, MD or similar) in genetics, molecular biology, or a related field.
3-5 years of professional medical writing experience in an industry setting, preferably in the 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.

Principal Medical Writer

Key skills