- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- ICON Clinical Research (Blue Bell, PA)
- Principal Medical Writer - United States (Remote) ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an ... future of clinical development. We have an incredible opportunity for a Principal Medical Writer to join ICON's Full Service team. The Principal Medical Writer … more
- 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
- 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
- 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
- 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
- Kelly Services (North Charleston, SC)
- **Technical Writer - 6-Month Contract (Fully Onsite)** **Location:** Morrisville, NC **Schedule:** Monday-Friday, 8:00 AM - 5:00 PM **Pay Rate:** $35-$45/hour ... **Type:** 6-Month Contract (Fully Benefited) We are seeking a **Technical Writer ** for a fully onsite, 6-month contract position with full benefits. The ideal… more
- Actalent (Largo, FL)
- Job Title: Technical Writer Job Description We are seeking a detail-oriented and technically proficient Technical Writer with a Quality Assurance (QA) background ... and end-user documentation to ensure product accuracy, usability, and regulatory compliance. Responsibilities + Develop and maintain high-quality documentation… more
- 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
- 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
- University of Colorado (Aurora, CO)
- **Quality Control Analyst I Data Reviewer/Technical Writer ** **Description** **University of Colorado Anschutz Medical Campus** **Department: Gates Biomanufacturing ... Facility** **Job Title: Quality Control Analyst I - Data Reviewer/Technical Writer ** **Position #: 803791 - Requisition #:37813** **Job Summary:** Key… more
- Nanobiosym, Inc. (Cambridge, MA)
- Cambridge, MA, USA | Contract Job Title: Scientific Writer (Onsite Consultant)Location: Cambridge, MA About the Role: We are seeking an experienced Scientific ... Writer with a strong background in scientific editing and...objectives. + Translate technical research into accessible content for regulatory submissions, funding bodies, and public communication. + Review… more
- ThermoFisher Scientific (Wilmington, NC)
- …Standard (Mon-Fri) **Environmental Conditions** Office **Job Description** **Senior Medical Writer (NA) (FSP; Remote)** At Thermo Fisher Scientific, you will ... - now and in the future. **Summarized Purpose:** We are looking for a Senior Medical Writer to work embedded with one of our clients in the FSP space; experience in… more