• ADC Therapeutics SA (New Providence, NJ)
    …10+ years of oncology clinical research experience as a clinical or regulatory medical writer within the pharmaceutical industry. Experience writing/leading the ... and edit documents used to support clinical trial conduct and reporting, regulatory interactions and submissions, including but not limited to: Develops directly or… more
    Upward (07/14/25)
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  • United Rentals, Inc. (Valley Cottage, NY)
    …You will play a key role in customer satisfaction, operational efficiency, and regulatory compliance. Key Responsibilities: Service Writer Duties: Manage Due for ... equipment rental provider, come build your future with United Rentals! SERVICE WRITER /TITLE CLERK: This dual-role position is responsible for managing rental service… more
    Upward (07/04/25)
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  • Innova solutions (Santa Monica, CA)
    A client of Innova Solutions is immediately hiring for a Technical Writer - II As an Technical Writer - II you will: Job Summary: We are seeking a skilled ... Technical Writer to create and maintain documentation related to Protected...guidelines, and healthcare quality standards. *Collaborate with healthcare professionals, regulatory experts, and other stakeholders to gather information and… more
    Upward (07/25/25)
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  • TSR Consulting (New Castle, DE)
    …and consultant will be treated with respect and professionalism. AML SAR WRITER Job Description Location: New Castle, Delaware Type: Contract Job #82765 Our ... client, a leading financial services company is hiring an AML SAR WRITER on a long-term contract basis. Job ID 82765 Work Location: New Castle, DE Summary: The AML… more
    Upward (07/21/25)
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  • Mindlance (Jersey City, NJ)
    …individual to join our Medical Writing team. In the Senior Medical Writer role, you will be responsible for independently leading document development by ... authoring and editing of medical and regulatory writing deliverables that support the Eikon clinical portfolio. You will partner with cross functional colleagues… more
    Upward (07/20/25)
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  • Bee Talent Solutions (Bellevue, WA)
    …seeking a Contractor to provide the following services: The Nuclear Operations Procedure Writer reports directly to the Procedure Manager and is focused on the ... NRC regulations, INPO accreditation criteria, and other codes, standards, and regulatory requirements. Provides regular training and mentoring to company personnel… more
    Upward (07/26/25)
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  • CACI International, Inc. (Washington, DC)
    Technical Writer - AWS Cloud Migration Job Category: Engineering and Technical Support Time Type: Part time Minimum Clearance Required to Start: Public Trust ... US Attorneys cases. We are seeking a half-time detail-oriented and highly skilled Technical Writer to join the CACI team. The ideal candidate will be responsible for… more
    Upward (07/05/25)
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  • Abbott (Minneapolis, MN)
    Title: Medical Writer III Location: Plymouth, MN Duration: 12 Months 100% Onsite Summary: This position works out of our Plymouth, MN location, supporting our ... Electrophysiology medical device division. The primary focus of the Senior Medical Writer role will be the development of scientific manuscripts for peer-reviewed… more
    Upward (07/14/25)
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  • Chickasaw Nation Industries, Inc. (CNI) (Rockville, MD)
    The Technical Writer - Training Development provides support to the agency by developing and fully executing new Standard Operating Procedures (SOP's). This position ... to assist other team members as needed. Resolves technical, grammatical, and regulatory compliance issues in documentation and graphic. Responsible for adherence to… more
    Upward (07/07/25)
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  • Tata Consultancy Service Limited (Naperville, IL)
    Must Have Technical/Functional Skills - Awareness of Regulatory guidelines (PhrMA, IFPMA, USFDA-OPDP, MHRA, EMA etc) for Product promotion, Advertising Standards ... and Copyright laws - A firm understanding of the regulatory landscape of the US Roles & Responsibilities *Perform...the US Roles & Responsibilities *Perform exhaustive Medical and Regulatory review of content respect to ensure Medical and… more
    Upward (07/19/25)
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  • LanceSoft (St. Paul, MN)
    …publication, scientific conference presentation) while ensuring compliance with regulatory , medical society, and corporate standards. Interface with physicians, ... clinical leadership, and other stakeholders to align evidence dissemination activities and deliverables. Lead, coordinate, and/or participate in Publication Committee meetings and administer follow-up actions (eg, document decisions). Support team activities… more
    Upward (07/10/25)
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  • Solomon Page (North Chicago, IL)
    We are currently hiring multiple experienced Principal Medical Writers to support regulatory writing efforts across all phases of clinical development (Phase I-IV) ... hoc, part-time, or full-time engagements. Responsibilities: Author and manage regulatory submission documents including INDs, NDAs, protocols, investigator brochures… more
    Upward (07/10/25)
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  • GZA GeoEnvironmental (Glastonbury, CT)
    …will have a strong background in Environmental, Health, and Safety Regulatory Compliance consulting. This position requires excellent leadership qualities, with a ... Safety Auditing Experienced EHS Trainer Industrial Hygiene Experience Experienced Technical Writer Qualifications: Desire to lead and grow a technical EHS practice… more
    Upward (07/06/25)
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  • Zoetis, Inc. (Kalamazoo, MI)
    …operating procedures (SOPs) and safety guidelines, as well as applicable regulatory standards, such as current Good Manufacturing Practices (cGMPs) *Operate, ... SOP's/OJT's- equipment, process, paperwork *Experience in working with Tech Writer , creating and maintaining training documentation Physical and Time requirements:… more
    Upward (07/23/25)
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  • AECOM (Pittsburgh, PA)
    …and regulations. Strong communication skills in coordinating with clients, sub-consultants, regulatory agencies, and members of the public to accomplish assigned ... and methods. Self-starter and ability to take initiative. Experienced technical writer . Additional Information This position does not offer relocation assistance.… more
    Upward (07/24/25)
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  • Battelle (Columbus, OH)
    …substances and evaluate their effects on human health. The technical report writer and study director will support scientific research that safeguards public health, ... Participates in all required training. Follows FDA GLP and other appropriate regulatory (eg, OECD, ICH) requirements to ensure all experimental data, including… more
    Upward (06/26/25)
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  • FSP Senior Regulatory Medical Writer

    ThermoFisher Scientific (Greenville, NC)
    …and are seeking candidates based in the US! As a remote-based Senior Medical Writer within the FSP team, you will provide high-quality medical and scientific writing ... will possess the versatility to author both clinical and preclinical regulatory documents, with therapeutic area expertise in infectious diseases and/or oncology.… more
    ThermoFisher Scientific (07/18/25)
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  • Senior Medical Writer

    BeOne Medicines (Emeryville, CA)
    …Required: + At a minimum 4 years' relevant industry experience as a regulatory medical writer with a BA/BS degree; PhD/PharmD in life sciences ... **General Description:** The Senior Medical Writer is responsible for writing, editing, and formatting... is responsible for writing, editing, and formatting clinical regulatory documents that conform to domestic and/or international … more
    BeOne Medicines (05/07/25)
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  • Nuclear Procedure Writer (U-Metal)

    Nuclear Fuel Services (Erwin, TN)
    …the safe operation of equipment, procedure flow and usability, and adherence to regulatory requirements and writer 's guidelines. + Interface with Subject Matter ... us on LinkedIn, X, Facebook and Instagram. Nuclear Procedure Writer (U-Metal) - Nuclear Fuel Services - Erwin, TN...Nuclear Fuel Services operations. In this position, the procedure writer will work with limited supervision to analyze, design… more
    Nuclear Fuel Services (07/14/25)
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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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