Full-Time Medical Writing Manager

Medical Writing Manager, Publications will play a crucial role in the development, tracking, and communication of scientific and clinical research findings related to precision oncology research. This individual will work closely with the cross-functional teams, including the MSL team, researchers, clinicians, external authors, and other stakeholders to produce high-quality, accurate, and compliant documentation, including research manuscripts, abstracts, clinical study reports, and other scientific communications.

1. Write, edit, and review scientific manuscripts, abstracts, posters, presentations, and other documents for publication in peer-reviewed journals and presentation at scientific conferences.
2. Conduct thorough literature reviews to support the development of research projects and clinical studies.
3. Collaborate with cross-functional team members (MSLs, researchers, clinicians, statisticians, external authors, etc.) to ensure the accuracy and clarity of scientific content.
4. Ensure all documents comply with regulatory guidelines, ethical standards, and company policies.
5. Manage multiple writing projects simultaneously, ensuring timely completion and adherence to deadlines.
6. Participate in quality control and review processes to ensure accuracy and integrity of all written materials.

Qualifications:

• Typically requires a university degree and 8 years of related experience; 6 years and a Master’s degree; 3 years and a PhD; or PharmD/MD.
• Exceptional writing, editing, and proofreading skills within Oncology and/or Diagnostics field.
• Strong understanding of scientific research methodologies and clinical trial processes.
• Proficiency in literature search databases and reference management software.
• Excellent project management and organizational skills.
• Understanding of journal requirements for publications.
• Ability to work independently and collaboratively in a fast-paced environment.
• Attention to detail and commitment to producing high-quality work.
• Experience in diagnostics or oncology research.
• Publication record in peer-reviewed journals.
• Knowledge of statistical analysis and data interpretation.
• Experience with medical writing software and tools.

Work Model:

Hybrid, with defined in-person/onsite and work-from-home days.

Salary:

US base salary range: $157,800 to $213,030 (full-time)

Benefits and other factors: The range does not include benefits, and if applicable, bonus, commission, or equity.

Additional Information:

• May be required to lift office supplies and use office equipment.
• Majority of the work is performed in a desk/office environment.
• Potential exposure to high noise levels, fumes, and biohazard material in the laboratory environment.
• Ability to sit for extended periods.

Commitment to Inclusivity: Guardant Health is committed to providing reasonable accommodations.

Equal Opportunity Employer: All qualified applicants will receive consideration for employment without regard to protected characteristics.

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