Technical Writing Director jobs in Boston, MA

Technical Writing Director establishes and plans the overall policies and goals for technical writing function. Develops standard documentation methods to effectively communicate product concepts and technical information. Being a Technical Writing Director coordinates with other teams and departments to determine technical writing needs. Requires a bachelor's degree. Additionally, Technical Writing Director typically reports to a senior manager or top management. The Technical Writing Director typically manages through subordinate managers and professionals in larger groups of moderate complexity. Provides input to strategic decisions that affect the functional area of responsibility. May give input into developing the budget. Capable of resolving escalated issues arising from operations and requiring coordination with other departments. To be a Technical Writing Director typically requires 3+ years of managerial experience. (Copyright 2024 Salary.com)

Recently Added Technical Writing Director jobs

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Manager, Technical Writing, CMC
  • Xenon Pharmaceuticals Inc.
  • Boston, MA FULL_TIME
  • Who We Are:
    Xenon Pharmaceuticals (NASDAQ: XENE) is a neuroscience-focused biopharmaceutical company committed to discovering, developing, and commercializing innovative therapeutics to improve the lives of people living with neurological and psychiatric disorders. We are looking for great people who thrive in a respectful, collaborative, inclusive, and productive culture to join the Xenon team.

    What We Do:
    We are advancing an exciting product pipeline to address indications with high unmet medical need, including epilepsy and depression. Our flagship XEN1101 program represents the most advanced potassium channel modulator in clinical development for multiple indications. Building upon the positive results and compelling data from our XEN1101 Phase 2b “X-TOLE” study in adult patients with focal epilepsy, our XEN1101 epilepsy program includes multiple Phase 3 clinical trials in patients with focal onset seizures and primary generalized tonic clonic seizures. In 2024, we are planning to initiate a Phase 3 XEN1101 program in major depressive disorder, based on topline data from our XEN1101 Phase 2 “X-NOVA” clinical trial. In addition, we are proud of the leading-edge science coming out of our discovery labs, including early-stage research programs that leverage our extensive ion channel expertise and drug discovery capabilities to identify validated drug targets and develop new product candidates. Backed by a strong balance sheet to support our growth plans, we continue to build a fully integrated, premier neuroscience company with strong discovery, clinical development, corporate, and commercial operations.

    About the Role:
    We are seeking a Manager, Technical Writing, CMC to join our growing team. The ideal candidate should be an independent and self-directed contributor who will be responsible for converting scientific data into clear, scientifically sound, well-structured scientific, technical, and regulatory documents intended for global health authorities and internal and external stakeholders. The Manager, Technical Writing, CMC, will author and manage the review and approval of CMC regulatory documents, including Module 2 and Module 3 CMC regulatory submissions, technical reports, and SOPs in close collaboration with critical functions within the CMC function.
    This position reports to the Senior Director, Regulatory Affairs, CMC and will be in Vancouver, BC, Canada or Boston, MA, USA. We will consider other jurisdictions for exceptional candidates. The level of the position will be commensurate with the candidate’s education and industry experience.

    RESPONSIBILITIES:
    • Author and edit the CMC sections of regulatory filings across all assets and clinical and commercial phases, including Module 2 & 3 submissions, IND/IMPDs, marketing applications, supplements, amendments, and annual reports, as needed.
    • Plan, manage and execute the authoring and review of CMC regulatory documents and deliver on timelines for submissions.
    • Manage and contribute strategy to responses to CMC queries and Requests for Information received from global health authorities.
    • Summarize scientific information from development reports and identify details relevant to regulatory clinical and commercial phase submissions supporting regulatory strategy.
    • Review documents for consistency and quality.
    • Develop processes and best practices to facilitate organization of information in preparation for clinical and marketing applications for Xenon products.
    • Act in accordance with Company policies, including, for example, the Code of Business Conduct and Ethics and ensure policies are understood and followed.
    • Other duties as assigned.
    QUALIFICATIONS:
    • A Bachelor’s or Master’s degree in pharmaceutical/life sciences, technical or medical writing, or a related field is strongly preferred.
    • 5 years working in the pharmaceutical industry, with an emphasis on authoring CMC regulatory content.
    • Proficiency in evaluating data, summarizing reports, authoring, and reviewing documents, and communicating results to internal and external stakeholders.
    • Extensive knowledge of eCTD structure and subsections.
    • Demonstrated, hands-on experience, managing and preparing regulatory submissions including INDs/CTAs and/or marketing applications, supplements and variations.
    • Proficiency with Microsoft Excel, PowerPoint, Project, and Word programs.
    The base salary range for this role is $101,900 to $123,400 USD; we will consider above this range for exceptional candidates. Base salary is determined by a combination of factors including, but not limited to, education and other qualifications, years of relevant experience, and internal equity.

    Our Total Rewards program includes base salary, target bonus, and stock options, as well as a full range of benefits including medical, dental, vision, short-& long-term disability, accidental death & dismemberment, and life insurance programs, Employee Assistance Program, travel insurance, and retirement savings programs with company matching contributions.
    Xenon encourages time to rest and re-charge through vacation, personal days, sick days, and an end-of-year company shutdown. Xenon highly values employee development and has an expanding Training, Learning & Development program, including a Tuition Assistance program for advanced degrees.
    To apply for this position, click Apply Now to complete the application. We thank all applicants for their interest; however, due to the volume of applicants, only those chosen for interview will be contacted.
  • 15 Days Ago
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Manager, Technical Writing, CMC
  • xenon
  • Boston, MA FULL_TIME
  • Who We Are: Xenon Pharmaceuticals (NASDAQ:XENE) is a neuroscience-focused biopharmaceutical company committed to discovering, developing, and commercializing innovative therapeutics to improve the liv...
  • 15 Days Ago
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Director, Medical Writing
  • TSP (A Syneos Health Company)
  • Waltham, MA FULL_TIME
  • Description The Role: Our client is looking for a motivated and experienced medical writer to join the team at a Director level. This role will be a strategic partner to teams and responsible for effi...
  • 19 Days Ago
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Associate Director, Medical Writing
  • Enanta Pharmaceuticals
  • Watertown, MA FULL_TIME
  • Job Summary: The Medical Writer will lead medical writing activities for clinical documentation preparation to support the advancement of clinical-stage programs. Primary Responsibilities: Coordinate ...
  • 22 Days Ago
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Associate Director, Medical Writing
  • Nuvalent, Inc.
  • Cambridge, MA FULL_TIME
  • The Role: Nuvalent is seeking a highly-motivated, results-oriented team member to join our growing organization as Associate Director, Medical Writing. This role, which will report to the VP, Clinical...
  • Just Posted
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Senior Director, Medical Writing
  • Apellis Pharmaceuticals, Inc.
  • Waltham, MA FULL_TIME
  • Position Summary: Apellis is seeking a Senior Director, Medical Writing (MW) to lead the MW, editing, and clinical publishing groups in support of a variety of regulatory areas including CMC and non-c...
  • 1 Day Ago
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0 Technical Writing Director jobs found in Boston, MA area

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Part-Time A/V TriCaster Technical Director / Operator
  • Armenian Cultural Asscoiation of America
  • Watertown, MA
  • We are looking for an entry-level TriCaster Technical Director / Operator. We specialize in live-streaming video project...
  • 4/26/2024 12:00:00 AM
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Director, Technical Program Management (Remote Eligible)
  • Capital One
  • Boston, MA
  • Center 1 (19052), United States of America, McLean, Virginia Director, Technical Program Management (Remote Eligible) Ar...
  • 4/25/2024 12:00:00 AM
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Senior Director, Technical Customer Support - Americas Boston, MA
  • Cybereason Inc.
  • Boston, MA
  • **Senior Director, Technical Customer Support - Americas** at Cybereason Boston, MA We are a company that wins as one. W...
  • 4/23/2024 12:00:00 AM
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Director, Technical Program Management - Enterprise Data
  • Capital One
  • Cambridge, MA
  • Center 3 (19075), United States of America, McLean, Virginia Director, Technical Program Management - Enterprise Data Ab...
  • 4/22/2024 12:00:00 AM
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Director, Technical Program Management - Enterprise Data
  • Capital One
  • Worcester, MA
  • Center 3 (19075), United States of America, McLean, Virginia Director, Technical Program Management - Enterprise Data Ab...
  • 4/22/2024 12:00:00 AM
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Director, Technical Program Management - Enterprise Data
  • Capital One
  • Taunton, MA
  • Center 3 (19075), United States of America, McLean, Virginia Director, Technical Program Management - Enterprise Data Ab...
  • 4/22/2024 12:00:00 AM
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Director, Technical Program Management (TPM), Cyber Intelligence
  • Capital One
  • Boston, MA
  • Center 2 (19050), United States of America, McLean, Virginia Director, Technical Program Management (TPM), Cyber Intelli...
  • 4/22/2024 12:00:00 AM
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Director, Technical Program Management (TPM), Cyber Intelligence
  • Capital One
  • Cambridge, MA
  • Center 2 (19050), United States of America, McLean, Virginia Director, Technical Program Management (TPM), Cyber Intelli...
  • 4/22/2024 12:00:00 AM
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About Boston, Massachusetts

Boston has an area of 89.63 square miles (232.1 km2)—48.4 square miles (125.4 km2) (54%) of land and 41.2 square miles (106.7 km2) (46%) of water. The city's official elevation, as measured at Logan International Airport, is 19 ft (5.8 m) above sea level. The highest point in Boston is Bellevue Hill at 330 feet (100 m) above sea level, and the lowest point is at sea level. Situated onshore of the Atlantic Ocean, Boston is the only state capital in the contiguous United States with an oceanic shoreline. Boston is surrounded by the "Greater Boston" region and is contiguously bordered by the citi...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Technical Writing Director jobs
$183,809 to $228,879
Boston, Massachusetts area prices
were up 2.5% from a year ago
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What does a Technical Writing Director do?

Technical Writing Director in Saint Cloud, MN
During the 20th century, the need for technical writing skyrocketed, and the profession finally became officially recognized.
December 11, 2019
Technical Writing Director in Cincinnati, OH
This results in technical documents, user manuals, technical reports, and instruction manuals.
December 09, 2019
Technical Writing Director in Vineland, NJ
Visit the Rutgers Business & Technical Writing Facebook page.
January 31, 2020
You will learn how to write different technical reports, e.g., laboratory reports, research reports, design and feasibility reports, progress reports, consulting reports, etc.
February 04, 2020