Medical Writer

MEDICAL WRITER ABOUT US: Biodesix is a leading diagnostic solutions company, driven to improve clinical care and outcomes for patients. Biodesix Diagnostic Tests support clinical decisions to expedite personalized care and improve outcomes for patients with lung disease. Biodesix Development Services enable the world’s leading biopharmaceutical, life sciences, and research institutions with scientific, technological, and operational capabilities that fuel the development of diagnostic tests, tools, and therapeutics. Our Mission : Transform patient care and improve outcomes through personalized diagnostics that are timely, accessible, and address immediate clinical needs. Our Vision : A world where patient diseases are conquered with the guidance of personalized diagnostics. For more information, please visit www.biodesix.com THE ROLE: The Medical Writer is responsible for developing, writing, editing, coordinating, and submitting scientific publications that communicate clinical, health economics and outcomes research (HEOR), and translational science data. This role partners closely with Clinical Development, Medical Affairs, HEOR, Biostatistics, investigators, and external authors to ensure scientific materials are accurate, compliant, timely, and aligned with Biodesix strategic objectives. The Medical Writer manages publication planning, correspondence with authors, manuscript development, conference abstracts, and submission activities while ensuring adherence to applicable publication standards and ethical guidelines. WHAT YOU'LL DO: Draft, edit, and finalize scientific abstracts, manuscripts, posters, presentations, and other scientific communications for conferences and peer-reviewed publications. Translate complex clinical, scientific, and health economics data into clear, accurate, and compelling scientific content suitable for target audiences. Collaborate with internal stakeholders, investigators, external authors, and subject matter experts to develop publication strategies and content. Manage publication timelines, milestones, deliverables, and submission schedules across multiple concurrent projects. Coordinate review cycles, consolidate reviewer comments, and incorporate feedback while maintaining document quality and scientific integrity. Prepare publication packages and support manuscript and abstract submissions to journals and scientific conferences, including compliance with formatting and submission requirements. Manage publication documentation, including author affiliations, disclosure forms, copyright agreements, acknowledgments, and approval records. Maintain publication databases, tracking tools, and document repositories to ensure audit readiness and organizational transparency. Support responses to journal reviewers, editorial comments, revision requests, and publication inquiries. Ensure all publications comply with Good Publication Practice (GPP), International Committee of Medical Journal Editors (ICMJE) recommendations, company policies, and applicable regulatory requirements. Operates independently with minimal supervision while managing multiple publication projects. WHAT YOU'LL BRING: Exceptional scientific and technical writing, editing, and proofreading skills. Strong understanding of clinical research, medical terminology, and scientific publication processes. Ability to synthesize complex scientific data into clear and concise communications. Strong project management and organizational skills with the ability to manage multiple priorities and deadlines. Excellent attention to detail and commitment to accuracy. Effective collaboration and stakeholder management skills in a cross-functional environment. Experience working with publication management systems, manuscript submission platforms, and document control processes. Knowledge of publication ethics, authorship standards, and disclosure requirements. Demonstrated ability to maintain confidentiality and handle sensitive clinical and scientific information. EDUCATION & EXPERIENCE: Bachelor's degree in Life Sciences, Biology, Clinical Research, Public Health, Pharmacy, Medical Writing, or related scientific discipline required. Advanced degree (MS, MPH, PharmD, PhD, or equivalent) preferred. Minimum 3 years of medical writing experience within biotechnology, diagnostics, pharmaceuticals, contract research organizations, medical communications agencies, or related healthcare environments. Demonstrated experience authoring or supporting peer-reviewed manuscripts, conference abstracts, scientific posters, and presentations. Experience working with clinical study reports, protocols, statistical outputs, and scientific datasets preferred. Knowledge of ICMJE recommendations, Good Publication Practice (GPP) guidelines, and scientific publication standards required. WHAT YOU'LL GET: Competitive base salary: $90,000 - $130,000 Discretionary bonus opportunity Comprehensive health coverage: Medical, Dental, and Vision Insurance: Short/Long Term Disability and Life Insurance Financial benefits: 401(k), Flex Spending Account 120 hours annual vacation 72 hours paid sick time 11 paid holidays + 3 floating holidays Employee Assistance Program Voluntary Benefits Employee recognition program Biodesix is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status. #li-remote #LI-FULLTIME