- BeOne Medicines (Emeryville, CA)
- **General Description:** The Senior Medical Writer is responsible for writing, editing, and formatting clinical regulatory documents that conform to domestic ... + At a minimum 4 years' relevant industry experience as a regulatory medical writer with a BA/BS degree; PhD/PharmD in life sciences preferred. All qualified… more
- ThermoFisher Scientific (Greenville, NC)
- **Work Schedule** Standard (Mon-Fri) **Environmental Conditions** Office **Job Description** **FSP Senior ** ** Regulatory ** **Medical Writer (** **Remote;** ... seeking candidates based in the US! As a remote-based Senior Medical Writer within the FSP team,...possess the versatility to author both clinical and preclinical regulatory documents, with therapeutic area expertise in infectious diseases… more
- Abbott (Maple Grove, MN)
- …or St. Paul, MN currently has an on-site opportunity for a ** Senior Medical Writer , Clinical Evaluation** . The Sr . Medical Writer on our Regulatory ... including Clinical Evaluation Plans/Reports, PMS and PMCF Plans/Reports, SSCPs, Regulatory Responses and other related documentation. + Evaluates and summarizes… more
- Lilly (Pleasant Prairie, WI)
- …site to provide safe and effective products and to meet customer expectations and regulatory requirements. The Senior Technical Writer is responsible for ... to deliver on new manufacturing investments and new pioneering technologies. The Senior Technical Writer serves as a site author to support GxP Documentation and… 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
- Terumo Neuro (Aliso Viejo, CA)
- **12933BR** **Title:** Sr . Medical Writer (US Remote & Temp to Hire) **Job Description:** **INNOVATION STARTS WITH YOU** Are you interested in working for an ... look at what **Micro** Vention (R) **TERUMO** has to offer. **Position Overview** The Sr . Medical Writer /Medical Writer will act as primary contact for… more
- Taiho Oncology (Princeton, NJ)
- …writing in a dynamic, collaborative, and cross functional environment. Position Summary: The Senior Medical Writer , Medical Writing is accountable for the timely ... delivery of high quality, regulatory -compliant documents including but not limited to protocols, IBs,...for the development of high-quality clinical documents submitted to Regulatory Authorities (eg FDA and EMA) including but not… more
- Parexel (Jefferson City, MO)
- The Senior Medical Writer will research, create, and edit all documents associated with clinical research. The Senior Medical Writer may operate as the ... to manage contributions of multiple writers working on related documents. The Senior Medical Writer also facilitates process improvement and technical… more
- Parexel (Frankfort, KY)
- **Company: Parexel is hiring an FSP - Senior Medical Writer with Structured Content Authoring experience to work Remotely.** **Location:** Remote (anywhere in US ... real impact on global health. **Role Summary** Parexel is seeking an experienced Senior Medical Writer to support the Structured Content Authoring (SCA)… more
- Vanguard (Malvern, PA)
- …how we can help both consultants and our mutual clients succeed. This senior marketing writer focuses on positioning, messaging, and marketing materials designed ... on that, and you'll work with marketing strategists and senior leaders to help expand our partnerships with consultants....from other 401(k) providers. We're looking for a creative writer who's comfortable managing complexity and ambiguity and can… more
- Abbott (Alameda, CA)
- …generic medicines. Our 114,000 colleagues serve people in more than 160 countries. ** Senior Technical Writer ** **Working at Abbott** At Abbott, you can do ... mothers, female executives, and scientists. **The Opportunity** We are seeking a Senior Technical Writer to lead the development of structured, user-friendly… more
- Parexel (Jefferson City, MO)
- **Job Summary:** The Senior Medical Writer will research, create, and edit all documents associated with clinical research. Responsibilities also include: acting ... to prepare, develop, and finalize clinical documents for submission to regulatory authorities, including but not limited to: briefing documents, investigator… more
- Houston Methodist (Houston, TX)
- At Houston Methodist, the Senior Scientific Writer is responsible for functioning as the mentor for junior staff with an extensive knowledge of both medical and ... ESSENTIAL FUNCTIONS** + Prepares moderately complex documents and sections of regulatory submissions and contributes scientific knowledge and analytical skills to… more
- Houston Methodist (Houston, TX)
- At Houston Methodist, the Senior Scientific Writer is responsible for functioning as the mentor for junior staff with an extensive knowledge of both medical and ... ESSENTIAL FUNCTIONS** + Prepares moderately complex documents and sections of regulatory submissions and contributes scientific knowledge and analytical skills to… more
- Noblis (Washington, DC)
- Responsibilities **Overview** We are seeking an experienced ** Senior Technical Writer /Editor** with a deep understanding of aviation operations, flight ... NAS operations, and flight procedures** to ensure technical accuracy and regulatory alignment. + Analyze existing and potential content to identify opportunities… more
- Guardian Life (Bethlehem, PA)
- …efficient operation of our Group Underwriting organization. As the Group Underwriting Senior Technical Writer in Group Benefits Underwriting, you will ... IT to gather source material and validate content. + Familiarity with regulatory standards and documentation practices in insurance. **You have:** + Proficiency in… more
- Flywheel Partners (New York, NY)
- …calls and client review meetings with Medical, Marketing, Sales, Legal, and Regulatory + Expertise in client business, brands, and organizational structure + ... Professional Development + Learn the Flywheel pathways for advancement within the Medical Writer track, or other roles based on interest and capabilities + Take… more
- Danaher Corporation (Miami, FL)
- Reagent Labeling Writer Intern Accelerating answers Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and ... about the Danaher Business System which makes everything possible. The Reagent Labeling Writer Intern will gain hands-on experience and exposure in the critical area… more
- MSys Inc. (Washington, DC)
- …and other departments to ensure all documents meet legal requirements and regulatory standards. + Ensure all documentation adheres to OCP established style guides ... and templates. + Conduct ongoing reviews of existing documentation to identify areas for improvement. + Produce quality documentation that is clear, consistent, appropriate, accurate, and meets procurement industry standards. + Organize and maintain documents… more
- GE HealthCare (Cleveland, OH)
- …plan product development and support release timelines + Support quality and regulatory teams with documentation creation and updates, applying knowledge of medical ... device guidelines + Collaborate with engineering teams to develop product copy for a clinical audience + Develop and maintain strong product knowledge for one or more product lines, understanding the competitive landscape What You'll Need: + At least 6 years… more