• Synterex (Boston, MA)
    …Management in leading the planning and preparation of high-quality clinical and regulatory documents. The medical writer may produce protocols, publications, ... Principal Medical Writer Synterex, Inc. is a global consortium of...with the requirements for preparation of key clinical and regulatory documents, including ICH and US/EMA regulatory more
    Upward (08/07/25)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …that all GMP documents are cutting edge and incorporate all latest regulatory and quality requirements.Track relevant KPIsEnsure periodic review of all GMP documents ... report authoringCollaborate with Protocol Coordinator to ensure appropriate Tech Writer support for required protocol activities.Assist with Audits, as… more
    HireLifeScience (09/23/25)
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  • Genius Road (Austin, TX)
    Procurement Analyst and RFP Writer Contract: 6-12 months Location: Austin, Texas (Hybrid - must already reside in the Austin area for consideration ) Our client is ... seeking an experienced Procurement Analyst / RFP Writer to support high-impact procurement efforts, including the development of complex Requests for Proposals… more
    Upward (08/01/25)
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  • RELI GROUP INC (Baltimore, MD)
    …critical programs. Position Summary: RELI Group is seeking a detail-focused Technical Writer to support the Information Security and Privacy Services (ISPS) under ... program transparency, stakeholder communication, and contract compliance. The Technical Writer will work closely with privacy, cybersecurity, risk management, and… more
    Upward (07/31/25)
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  • Senior Medical Writer , Global…

    Ascendis Pharma (Princeton, NJ)
    …within Medical Writing. Furthermore, you have: + Experience in authoring clinical/ regulatory documents. + Excellent verbal and written communication skills with the ... ability to effectively communicate with a variety of teams and individuals, across time zones. + Ability to understand, interpret and communicate data from clinical trials. + Proven ability to work with and lead cross-functional, global teams of contributors.… more
    Ascendis Pharma (07/17/25)
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  • Senior Medical Writer , Clinical Evaluation…

    Abbott (Maple Grove, MN)
    …for a **Senior Medical Writer , Clinical Evaluation** . The Sr. Medical Writer on our Regulatory Clinical Evaluation team provides technical and strategic ... including Clinical Evaluation Plans/Reports, PMS and PMCF Plans/Reports, SSCPs, Regulatory Responses and other related documentation. + Evaluates and summarizes… more
    Abbott (09/25/25)
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  • Service Writer / Title Clerk

    United Rentals (Bladensburg, MD)
    …will play a key role in customer satisfaction, operational efficiency, and regulatory compliance. **Key Responsibilities:** **Service Writer Duties:** Manage Due ... rental provider, **come build your future with United Rentals!** **SERVICE WRITER /TITLE CLERK:** This dual-role position is responsible for managing rental service… more
    United Rentals (08/30/25)
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  • Operations Procedure Writer (Nuclear)

    Xcel Energy (Welch, MN)
    …that the changes are technically accurate, applicable, and in conformance with regulatory requirements and applicable Operations Writer 's Guides. Further, the ... Operations procedures can be implemented without adversely affecting plant, personnel, or equipment safety. **Essential Responsibilities** + Use Document Control and Engineering Records to retrieve vendor manuals, references, prints, schematics, design… more
    Xcel Energy (09/26/25)
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  • Exam Writer

    Holtec International (Covert, MI)
    …and historic undertaking for the industry and the nation! JOB SUMMARY The Exam Writer develops and administers Regulatory Exams in accordance with NUREG 1021, ... Exam Writer Holtec Decommissioning International (HDI) is currently seeking...for assigned programs, including interfacing with INPO and Nuclear Regulatory Commission (NRC) as required. + Interacting professionally with… more
    Holtec International (09/12/25)
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  • Manager, CMC Regulatory

    Lilly (Philadelphia, PA)
    …development and/or manufacturing with a minimum of two years of CMC regulatory experience or related (eg CMC writer ) **Additional Skills/Preferences:** + ... through philanthropy and volunteerism. **Position Overview:** The Manager, Manager- CMC Regulatory is responsible for the preparation and delivery of high-quality… more
    Lilly (08/14/25)
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  • Medical Writer

    BD (Becton, Dickinson and Company) (Sparks, MD)
    **Job Description Summary** The Medical Writer develops scientific and medical communication materials within BD Diagnostic Solutions (DS), collaborating with ... exchange activities. As part of the MedComms team, the Medical Writer will focus on developing publication-ready content (including tables, figures, graphics,… more
    BD (Becton, Dickinson and Company) (10/07/25)
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  • Associate Director-Principal Medical Writer

    Sanofi Group (Morristown, NJ)
    **Job Title:** Associate Director-Principal Medical Writer **Location:** USA, Remote. Proximity to Cambridge/Boston, MA or Morristown, NJ is highly desirable for ... skills could be critical in helping our teams accelerate progress. The Principal Medical Writer is a key member of the Medical Writing team, the Clinical Trial Team… more
    Sanofi Group (09/06/25)
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  • Sr. Medical Writer (US Remote & Temp…

    Terumo Neuro (Aliso Viejo, CA)
    …years of scientific experience. 3. Demonstrated experience in the development of regulatory / clinical submissions (preferably as a medical writer for ... **12933BR** **Title:** Sr. Medical Writer (US Remote & Temp to Hire) **Job...job duties include: + Collaborating with the clinical & regulatory teams to write clinical documents for regulatory more
    Terumo Neuro (08/08/25)
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  • Senior/Medical Writer - Global Medical…

    United Therapeutics (Research Triangle Park, NC)
    …You Are You are creative and detail-oriented with deep expertise in regulatory submissions and writing, including clinical study reports, clinical study protocols, ... company where collaboration and adaptability are crucial to success. The Senior/Medical Writer will support Global Medical Affairs Phase 3b/4 research as well as… more
    United Therapeutics (09/05/25)
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  • Procedure Writer

    Salado Isolation Mining Contractors (Carlsbad, NM)
    Procedure Writer (186) Requisition ID **186** - Posted - **PI-TR Training & Procedures** - **Carlsbad, NM, US - WIPP Site** - **Administrative** **Overview** **Be ... candidate will obtain process specific training and follow the WIPP facility writer 's guide with respect to format, order, clarity, conciseness, style and… more
    Salado Isolation Mining Contractors (10/01/25)
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  • Principal Medical Writer

    ICON Clinical Research (Blue Bell, PA)
    Principal Medical Writer - Remote ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive ... shape the future of clinical development. We are currently seeking a Principal Medical Writer to join our diverse and dynamic team. As a Principal Medical Writer more
    ICON Clinical Research (09/30/25)
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  • Technical Writer

    Koniag Government Services (Washington, DC)
    …Solutions, LLC a Koniag Government Services company **,** is seeking a Technical Writer to support KMS and our government customer in Washington, DC. This position ... off, and more. Koniag Management Solutions, LLC is seeking a dedicated Technical Writer to support Federal IT Governance programs for our government customers. This… more
    Koniag Government Services (09/24/25)
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  • Staff UX Writer and Content Designer,…

    Google (New York, NY)
    Staff UX Writer and Content Designer, Trust, Core _corporate_fare_ Google _place_ New York, NY, USA **Advanced** Experience owning outcomes and decision making, ... working with legal partners or in a compliance or regulatory space. + Experience in influencing product strategy with...with cross-functional stakeholders. **About the job** As a UX writer , you are an advocate for Google design, shaping… more
    Google (10/02/25)
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  • Pharma Technical Writer

    System One (New Brunswick, NJ)
    Job Title: Pharma Technical Writer Location: New Brunswick, NJ Hours/Schedule: Mon-Friday (normal business hours) Compensation: $34.87- $44.29 Type: Contract ... Overview Leading pharmaceutical company looking for an experienced Technical Writer . Ideal candidates should have at least 2 years of experience specifically for … more
    System One (09/23/25)
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  • CER Technical Writer

    Kelly Services (Raynham, MA)
    **CER Technical Writer ** The CER Technical Writer must have experience within the medical device industry and knowledge of clinical evaluation report ... regulatory requirements, evidence generation, and CER document creation to...in accordance with local procedures, the client's guidelines and regulatory requirements + Ensures the CER and SSR files… more
    Kelly Services (10/03/25)
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