• Senior Medical Writer

    Flywheel Partners (New York, NY)
    …effective communicators, and detail-oriented professionals. We are searching for a senior medical writer (aka scientific writer , content developer) with ... Lead scheduled status calls and client review meetings with Medical , Marketing, Sales, Legal, and Regulatory +...+ Learn the Flywheel pathways for advancement within the Medical Writer track, or other roles based… more
    Flywheel Partners (11/08/24)
    - Save Job - Related Jobs - Block Source
  • Principal Medical Writer - Oncology

    Merck (Columbus, OH)
    …The Principal Medical Writer is responsible for leading medical writing deliverables that support the clinical regulatory writing portfolio. The ... Medical Writer : + Independently leads and authors clinical regulatory documents (eg, protocols, pivotal clinical study reports, clinical sections of… more
    Merck (11/20/24)
    - Save Job - Related Jobs - Block Source
  • Medical Writer

    Actalent (Bethesda, MD)
    Clinical Research Medical Writer Our client is seeking an entry-level Medical Writing Associate to join their team and assist with various duties related to ... + Prepare or assist in the preparation of drafting medical , scientific, and regulatory documents, SOPs, and...and Wednesday or Tuesday and Thursday. Fridays are always remote . About Actalent Actalent is a global leader in… more
    Actalent (11/13/24)
    - Save Job - Related Jobs - Block Source
  • Solid Waste Permit Writer

    State of Indiana (Indianapolis, IN)
    Solid Waste Permit Writer Date Posted: Nov 20, 2024 Requisition ID: 452475 Location: Indianapolis, IN, US, 46204 Work for Indiana Begin a fulfilling career with the ... Section. In this role you will be a permit writer responsible for reviewing permit applications to determine if...violations of state and federal regulations. Provides technical and regulatory guidance to the regulated community in their assigned… more
    State of Indiana (11/20/24)
    - Save Job - Related Jobs - Block Source
  • Technical Writer (Scientific Writing)…

    MD Anderson Cancer Center (Houston, TX)
    …the public. **SUMMARY** Writes, edits and coordinates production of highly technical medical material. Retrieves data from databases and other internal and external ... patient education/materials, IRB forms. Works collaboratively with research nurse manager and regulatory staff to develop or coordinate the development of the study… more
    MD Anderson Cancer Center (09/07/24)
    - Save Job - Related Jobs - Block Source
  • Associate Customs Entry Writer (2-11pm EST)

    CH Robinson (Wood Dale, IL)
    CH Robinson is seeking an **Associate Customs Entry Writer ** to join our Global Forwarding division. As a key player on our customs team, you'll navigate the ... skills, master the art of precise data management, and deepen your regulatory knowledge. If you are organized, possess exceptional communication abilities, and… more
    CH Robinson (11/20/24)
    - Save Job - Related Jobs - Block Source
  • Procedure Writer - Hope Creek Maintenance…

    PSEG (Salem County, NJ)
    …location categories: onsite roles, hybrid roles that are a blend of onsite and remote work, remote local roles that are primarily home-based but require some ... of purpose-driven in-person interaction and living within a commutable distance, and remote non-local roles that can be effectively performed remotely with the… more
    PSEG (10/31/24)
    - Save Job - Related Jobs - Block Source
  • UX Writer , Vehicle Interface

    General Motors (Columbus, OH)
    **Job Description** ** Remote OR Hybrid:** Reporting where work can/needs to be performed / collaboration should happen. If the person lives w/n 50 miles of such a ... content and adherence to writing standards. + Stay informed about regulatory requirements and industry standards related to in-vehicle content and ensure… more
    General Motors (11/26/24)
    - Save Job - Related Jobs - Block Source
  • Director, Regulatory Medical Writing…

    J&J Family of Companies (Spring House, PA)
    Johnson & Johnson is currently seeking a Director, Regulatory Medical Writing. The primary location for this position is the United States. Secondary locations ... At Johnson & Johnson, we all belong. The Director, Regulatory Medical Writing (RegMW) is a highly... Medical Writing (RegMW) is a highly experienced medical writer and influential leader with strategic… more
    J&J Family of Companies (11/22/24)
    - Save Job - Related Jobs - Block Source
  • Sr. Scientist, Medical Writing and Product…

    Cardinal Health (Columbus, OH)
    …discipline, preferred. + Ideally targeting 5+ years of experience as a medical writer preparing regulated documents in the pharmaceutical and/or biotech ... **_What Medical Writing and Product Development ( Regulatory )...Brochures, and briefing books, among others. **Location -** Fully remote (work hours will be 8am - 5pm in… more
    Cardinal Health (11/22/24)
    - Save Job - Related Jobs - Block Source
  • Senior Associate Director, Strategic Content

    Dana-Farber Cancer Institute (Brookline, MA)
    …positive, results-oriented culture founded on open communication. This position is considered remote , 0-1 days onsite at 10 Brookline Place, Brookline, MA each week. ... physician/researchers, and we work with amazing partners, including other Harvard Medical School-affiliated hospitals. + Lead strategic content efforts to solicit… more
    Dana-Farber Cancer Institute (10/16/24)
    - Save Job - Related Jobs - Block Source
  • Clinical Trials Manager

    University of Colorado (Aurora, CO)
    …study concept document, study protocol and related documents. + Collaborates with the Medical Writer on clinical/scientific and regulatory documents. + Lead ... **Clinical Trials Manager** **Description** **University of Colorado Anschutz Medical Campus** **Department: Department of Medicine, Division of Allergy & Clinical… more
    University of Colorado (11/22/24)
    - Save Job - Related Jobs - Block Source
  • Associate Director, Clinical Scientist (Athero…

    Merck (Upper Gwynedd, PA)
    …the lead clinical scientist on the clinical trial team. + Collaborates with the Medical Writer on clinical/scientific and regulatory documents. Partners with ... during study start up (eg, database set up) Lead medical monitoring team in review and interpretation of clinical...ability to: + Apply strong knowledge of clinical research regulatory requirements (eg, GCP and ICH) + Manage multiple… more
    Merck (11/14/24)
    - Save Job - Related Jobs - Block Source
  • Director, Clinical Pharmacology

    IQVIA (Durham, NC)
    …teams that include Project Manager, CRA, Data Manager, Biostatistician, Programmer, and/or Medical Writer . + Maintain awareness of overall developments in the ... This position is Full-Time and Remote -based anywhere in the United States or Canada....sections of dossiers for product registration and communicate with regulatory agencies. + Ensure quality and timely delivery of… more
    IQVIA (10/26/24)
    - Save Job - Related Jobs - Block Source
  • Operations Specialist IV - Conduct of Operations…

    Amentum (Richland, WA)
    …and operation, including environmental, safety, and health aspects and regulatory conformance through completion and maintenance of assigned operations ... response procedures, and other operational documents to ensure they meet technical writer 's standards and are effectively implemented + Perform Facility walkdowns to… more
    Amentum (11/15/24)
    - Save Job - Related Jobs - Block Source
  • Technical Service Advisor- Hazardous Waste

    Republic Services (Elizabeth, NJ)
    …sales department to offer solutions that meet quality and regulatory standards, performs technical evaluations, facilitates communication between departments, ... a fast-paced environment. + Proficient with Microsoft Office, DocuSign, and PDF writer . **QUALIFICATIONS:** + Commitment to customer service and possess the ability… more
    Republic Services (11/22/24)
    - Save Job - Related Jobs - Block Source
  • Water Technical Leader

    AECOM (Manchester, NH)
    …experience + Strong communication skills in coordinating with clients, sub-consultants, regulatory agencies, and members of the public to accomplish assigned ... methods. + Self-starter and ability to take initiative. + Experienced technical writer . **Additional Information** + Relocation is not available for this position. +… more
    AECOM (10/03/24)
    - Save Job - Related Jobs - Block Source