• Sutro Biopharma (South San Francisco, CA)
    Description Sutro Biopharma, Inc. is looking for a Director, Regulatory Affairs Medical Writer who will provide leadership in development and execution of ... scientific writing and will work cross-functionally, advising the team on regulatory expectations for document content while maintaining compliance with global (FDA,… more
    Upward (07/14/25)
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  • The Planet Group (Paramus, NJ)
    Job Description Job Title: Pharmaceutical CMC Writer ( Regulatory Medical Writer ) Location: Hybrid in Paramus, NJ (3-4 days onsite/week) Employment Type: ... Rate: Up to $50.68/hr W2 Introduction Are you a detail-oriented Regulatory Medical Writer with a passion for pharmaceutical development and a strong… more
    Upward (07/20/25)
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  • Integrated Resources, Inc. (Santa Monica, CA)
    Job Title: Technical Writer - III Location: Santa Monica, CA (Hybrid) Duration: 6+ Months (Possible Extension) Pay range: $80/hr. on W2 Job Description: Client is ... motivated individual with late-phase CMC technical experience, including technical and regulatory submission experience. This position is part of the Process… more
    Upward (07/16/25)
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  • PSC Biotech (Irvine, CA)
    …and distributed to the highest standards, in compliance with all applicable regulatory requirements. Our goal is to skyrocket our clients' success, and you ... a job-it's about your career and your future. Your Role As a Technical Writer within our pharmaceutical manufacturing operations, you will play a pivotal role in… more
    Upward (07/29/25)
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  • Caesars Entertainment (Shelbyville, IN)
    …disputes by following posted house rules and working with local regulatory bodies to ensure compliance *Monitors competitors' practices and technological innovations ... tools available appropriately. *Ensures that departmental procedures conform to all regulatory requirements and provide maximum security for the company's assets.… more
    Upward (07/27/25)
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  • FreightTAS LLC (Cranford, NJ)
    Import Coordinator / Entry Writer - On-site Springfield, NJ Salary: $50,000 - $75,000 (based on experience and qualifications) Schedule: Monday-Friday, 8:30 AM - ... with a supportive, low-turnover culture Requirements Proven experience as a customs entry writer or in a similar role within logistics and supply chain. In-depth… more
    Upward (07/18/25)
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  • MannKind Corporation (Bedford, MA)
    …Position Summary: MannKind Corporation is seeking a detail-oriented and highly organized Medical Writer to join our team. The Medical Writer will provide ... and standards to enhance consistency and quality across all regulatory and scientific documents. Oversee the development and finalization of… more
    Upward (07/04/25)
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  • Lifelancer (Washington, DC)
    About the job Senior Medical Writer - UK/US - Remote Job Title: Senior Medical Writer - UK/US - Remote Job Location: Washington, DC, USA Job Location Type: ... liaises with Subject Matter Experts across the company, including regulatory strategists and clinical methodologists in high level protocol...Minimum of 4 years of experience as a Medical Writer or equivalent role as determined by management to… more
    Upward (07/26/25)
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  • RIT Solutions, Inc. (Allston, MA)
    …(SOP's, guidelines, validation master plans, etc.) to ensure compliance with regulatory requirements. *Be able to establish working relationships with other support ... and production areas in order to gather all the necessary information required. * Must be proficient in Veeva Vault with a working knowledge of templates, workflows and approval process . *Proficient in MS Word, Excel, PowerPoint and Outlook. more
    Upward (07/30/25)
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  • Allen Spolden (New Brunswick, NJ)
    Job Description The Medical Writer will primarily work on the development and delivery of high-quality documents such as Clinical protocols, protocol amendments, ... together with integrated summaries (ISS and ISE), and other related clinical/ regulatory documents to support Investigational New Drug Applications (IND), New Drug… more
    Upward (07/11/25)
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  • Michael Page (New York, NY)
    …Coordinate with cross-functional teams to ensure messaging consistency and compliance with regulatory standards. MPI does not discriminate on the basis of race, ... color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI… more
    Upward (07/13/25)
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  • Vonage (Washington, DC)
    …Ericsson. An exciting opportunity has arisen for an ambitious CFIUS Business Analyst and Writer to join the BCT Office. The CFIUS Business Analyst will play a ... Experience working within a federal government administrative law and or regulatory body Experience in managing compliance programs, developing compliance policies,… more
    Upward (07/11/25)
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  • Mindlance (New Castle, DE)
    …Location: New Castle, DE End date: 1/14/2026 Rate: /hr Role: AML SAR WRITER SAR writing exp is required** The AML Analysts within the CRIU review ... and preparing Suspicious Activity Reports (SARs) in accordance with applicable regulatory requirements preferred. *CAMS Certification is a plus *Knowledge of the… more
    Upward (07/19/25)
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  • Bayer (Whippany, NJ)
    …for pharmaceutical communications; Partners with Commercial, Medical, Legal and Regulatory colleagues to create effective communications programs aligned with ... and issues management experience; Excellent oral presentation and influence skills; Strong writer who can take complex information and produce clear, compelling, and… more
    Upward (07/19/25)
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  • Marten Law LLP (Washington, DC)
    …in advising global companies on how to address the evolving regulatory environment concerning sustainability reporting, climate-related targets and disclosures, due ... of experience in global sustainability and product law matters. Are an exceptional writer , with experience as the primary author of legal memoranda, briefs, motions,… more
    Upward (07/02/25)
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  • Arcus Biosciences (Hayward, CA)
    …drug product development Authoring technical development reports and authoring/contributing to regulatory filings Review and approval of internal and CDMO analytical ... functionality Collaborate with cross-functional CMC teams (including QA and Regulatory ) to achieve project goals Opportunities for analytical lead responsibility… more
    Upward (07/10/25)
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  • Fidelity Investments (Smithfield, RI)
    …customers with the right Fidelity products and services. As a UX Writer /Content Strategist, you'll play a key role in shaping customer experiences-helping people ... a strong portfolio that demonstrates your skills is essential. A versatile writer who can tailor messaging for diverse audiences-whether it's individual investors,… more
    Upward (07/12/25)
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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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  • 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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