Technical Writing Director jobs in New Jersey

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)

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Specialist 3 - Technical Writing
  • jnj
  • Hopewell, NJ FULL_TIME
  • Johnson & Johnson Family of Companies

    Title: Plain Language Summary Writer

    Location: Titusville, NJ (onsite)

    Duration: 6 months

    Benefits on offer for this contract position: Health Insurance, Life insurance, 401K and Voluntary Benefits

    Please note that this is a contract role providing services to the Johnson & Johnson Family of Companies through external staffing partners of Kelly OCG. If you are selected for this role, you will be employed by a contract staffing supplier and will not be a member of the Johnson & Johnson Family of Companies.

    Summary:

    Write and review plain language summaries of clinical trial results. Reviews Plain Language Summaries of clinical trial results to ensure compliance with internal policy, regulatory standards, and health literacy principles. Project requires PLS training.

    Responsibilities:

    • Assist vendor oversight, review of all draft PLSs, ensuring adherence to PLS compliance documents (i.e., PLS Template and Job Aid), providing feedback, follow-up, and documentation.
    • Assist in initiating and preparing for PLS production-related meetings (i.e., kick-off meetings, comment review meetings) with the study and standards team in accordance with existing procedures.
    • Ensures that results presentation is appropriate to the statistical analysis, and relevant for nonscientific readers, and includes sufficient context.
    • Attends and facilitates cross-functional discussions by proposing solutions on guidelines, standards, processes and to resolve content issues.
    • Assists project team members in developing material for the study team kick-off meetings, assists with training needs.
    • Experience in translating scientific content into easy-to-understand terms following well understood health literacy and numeracy principles. Sensitivity to the needs of lay audiences
    • Knowledge of the application of regulatory guidance (i.e., EU Clinical Trial Regulations) in writing PLSs
    • Understands the principles of clinical research, fundamental biostatistics, and safety data reporting.
    • Interprets information for indications across various therapeutic areas using source documents such as the protocol, Clinical Study Report but also the Informed Consent Forms, Technical Summaries of Clinical Trial Results (i.e., Clinicaltrials.gov, EudraCT)
    • Applies critical scientific thinking to align the study rationale and research objectives with study endpoints and results. Understands the trial design, disease characteristics and measures being summarized to ensure study results accurately present scientific content in plain language.
    • The role must master the use of systems, tools, and processes.
    • Has strong oral/written communication and presentation skills
    • Sound organizational and management skills, and the ability to balance multiple responsibilities and work under tight time constraints.

    Qualifications:

    • A university/college degree in relevant pharmaceutical/scientific experience is required.
    • A minimum of 3 years of relevant pharmaceutical/scientific experience in a clinical development environment (pharmaceutical, medical device, CRO or other clinical development service organization) is required.
  • 11 Days Ago

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Associate Director of Medical Writing
  • IPG Health
  • Hackensack, NJ FULL_TIME
  • Singular talents thrive as an Associate Director of Medical Writing with CMC Affinity. We advocate. We captivate. We cogently demonstrate. We combine gravitas with that lightness of touch that only co...
  • Just Posted

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Associate Director Regulatory Writing
  • Novartis
  • East Hanover, NJ FULL_TIME
  • 394328BR Associate Director Regulatory Writing USA About the role This is a remote position To write, review and/or handle the production of high quality clinical and safety documentation for submissi...
  • 11 Days Ago

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Director- Medical Writing
  • Katalyst Healthcares & Life Sciences
  • Princeton, NJ FULL_TIME
  • Company DescriptionKatalyst Healthcares & Life Sciences is hiring entry level candidates for several positions for contract research in Clinical trials of drugs, biologics and medical devices.We have ...
  • 12 Days Ago

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Associate Director, Medical Writing - Neuroscience
  • Integrated Resources INC
  • Woodcliff Lake, NJ FULL_TIME
  • Company DescriptionClient is a Large Pharmaceutical CompanyJob DescriptionThe Associate Director - Medical Writing will be the designated Lead Medical Writer for approximately 3 Neuroscience or Genera...
  • 13 Days Ago

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Executive Director, Global Scientific and Regulatory Medical Writing
  • Bristol Myers Squibb
  • Princeton, NJ FULL_TIME
  • Working with UsChallenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting ...
  • 12 Days Ago

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Technical Director
  • Univision Communications, Inc.
  • Teaneck, NJ
  • The Local New York Operations team at TelevisaUnivision in Teaneck, NJ is looking for an APC Technical Director to join ...
  • 3/28/2024 12:00:00 AM

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Technical Director
  • NetApp, Inc.
  • San Jose, CA
  • About NetApp We're forward-thinking technology people with heart. We make our own rules, drive our own opportunities, an...
  • 3/27/2024 12:00:00 AM

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Technical Director
  • University of California Berkeley
  • Berkeley, CA
  • About Berkeley At the University of California, Berkeley, we are committed to creating a community that fosters equity o...
  • 3/27/2024 12:00:00 AM

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Technical Director
  • Precision Castparts
  • Huntington, WV
  • Country 1 United States of America State / County 1 West Virginia City 1 Huntington Division 1 Energy Company 1 HBE Func...
  • 3/27/2024 12:00:00 AM

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Technical Director (Project)
  • RUN Studios
  • Redmond, WA
  • Description Since 2007, RUN Studios has created world-class creative content for prominent and emerging brands, bringing...
  • 3/27/2024 12:00:00 AM

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Technical Director Quality
  • MKS Instruments
  • Irvine, CA
  • Spectra-Physics, Ophir, Newport and ESI are brands within the MKS Instruments Photonics Solutions division. We provide a...
  • 3/27/2024 12:00:00 AM

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Technical Director / Editor
  • Cascade Hills Church
  • Columbus, GA
  • Job Description Job Description Cascade Hills Church in Columbus, Georgia is seeking an experienced Technical Director a...
  • 3/27/2024 12:00:00 AM

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Associate Technical Director
  • Gearbox Software
  • Frisco, TX
  • Associate Mobile Technical Director, Publishing Responsibilities: * Guide multiple teams through the mobile game develop...
  • 3/25/2024 12:00:00 AM

New Jersey is bordered on the north and northeast by New York (parts of which are across the Hudson River, Upper New York Bay, the Kill Van Kull, Newark Bay, and the Arthur Kill); on the east by the Atlantic Ocean; on the southwest by Delaware across Delaware Bay; and on the west by Pennsylvania across the Delaware River. New Jersey is often broadly divided into three geographic regions: North Jersey, Central Jersey, and South Jersey. Some New Jersey residents do not consider Central Jersey a region in its own right, but others believe it is a separate geographic and cultural area from the Nor...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Technical Writing Director jobs
$180,057 to $224,215

Technical Writing Director in Rockford, IL
Even though engineers are technical people, that doesn’t necessarily mean they are good technical writers.
January 10, 2020
Technical Writing Director in Wilmington, DE
Even in technical writing there is no excuse for that.
January 25, 2020
Technical Writing Director in Bradenton, FL
For example, a technical writing department may be expected to manage documentation and is necessary for process control, but you can add commitment to best-in-class performance, which communicates significance, to your writers and others.
December 21, 2019