Technical Writer I

About Flagship. At Flagship Biosciences, we are dedicated to improving the health of patients everywhere by pioneering the most advanced computational tissue image analysis, clinical support, and diagnostics services that help pharmaceutical companies develop the solutions to treat, manage, and cure the world's most challenging medical conditions. Flagship develops its analytic and infrastructural technology in-house, providing truly unique capabilities not available anywhere else in the market. None of this can be done without a strong, talented team of people dedicated to moving our business forward.

Our Cultural Values

• Smart and Hungry: We simplify complex problems. We are never satisfied and we love to learn.
• Find a Way: We find solutions for any problem. We must collaborate to win.
• Get the Right Stuff Done: The right strategy and execution to positively impact patients' lives.
• Respect: Open communication, refer to the expert but respect equal say at the table.

Job Classification - Full time, Exempt

Essential Job Functions

• Prepare (write and edit) analytical validation and clinical reports, summary documents, and other documents that will be submitted to partners and/or regulatory agencies for publication and/or presentation. May prepare scientific manuscripts, abstracts, and posters. May assist in literature research to support reports and scientific plans.
• Write, analyze, integrate, organize, and edit materials based on large amounts of disparate data from multiple sources.
• Provide writing, editing, and project management support for the development of clinical analytical documents and medical publications/presentations, as well as regulatory filings as needed. Assist in the development of formats, templates, review sheets, style guides and guidelines for clinical and other documentation.
• Edit and proofread to ensure technical accuracy, readability, usability, and persuasiveness. Review and revise materials to ensure consistency with other relevant, system-wide standards and practices. Proof and approve final copies for assigned projects. Apply knowledge of established stylistic rules, correct grammar and spelling, and use consistent tone and style to achieve educational objectives.
• Support a cross-functional team including Pathology, Science, Operations, and Quality/Regulatory.

Basic Requirements

• Bachelor's degree (advanced degree preferred) in life sciences with a writing background.
• 1-3 years of experience in medical, scientific or technical writing, including writing for both general public/patients and technical/business audiences.
• Excellent writing, editing, and information design skills, as well as attention to detail with demonstrated ability to translate complex information into clear, persuasive, and actionable materials.
• Demonstrated proficiency with computer systems and tools including word processing, spreadsheets, presentations, and desktop publishing applications.
• Demonstrated proficiency in medical and scientific information retrieval.
• Knowledge of medical terminology and medical writing conventions, including the use of abbreviations, citations, etc.
• Demonstrated excellent verbal and written communication skills and data analysis skills; ability to communicate tactfully and clearly with professionals at all levels.

Company Benefits

• Health (100% company-paid for employee only on the lowest base & HSA plan)
• Dental (100% company-paid for employee only)
• Vision (100% company-paid for employee only)
• Medical and dependent care FSA
• Company-paid STD & LTD
• Company-paid Basic Life & AD&D
• Voluntary life, AD&D, and accident insurance
• Generous PTO/Sick Leave & Flex PTO
• 8 company-paid holidays
• Paid-time off for bereavement, jury duty, voting
• 401k (match up to 4%)
• Employee assistance program
• Legal Shield & ID Shield
• Education assistance
• Professional development program
• 4 days in the office, 1 day remote