- California State University (Northridge, CA)
- College and Marketing Communications Writer Job no: 549159 Work type: Staff Location: Northridge Categories: Unit 9 - CSUEU - Technical Support Services, ... Duties Under general supervision, the College and Marketing Communications Writer creates foundational and compelling cases for programs, collaborates… more
- ThermoFisher Scientific (Greenville, NC)
- …(FSP) Team 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 ... will possess the versatility to author both clinical and preclinical regulatory documents, with therapeutic area expertise in infectious diseases and/or oncology.… more
- 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
- 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
- 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
- Teledyne (San Diego, CA)
- …want the excitement of being on a team that wins. **Job Description** Sr . Technical Writer **Summary Statement:** Researches, creates, and edits operational, ... internal guidelines by utilizing skills as a seasoned, experienced technical writer with a full understanding of industry standards/practices for technical… more
- Prime Therapeutics (Springfield, IL)
- …that. It fuels our passion and drives every decision we make. **Job Posting Title** Senior Proposal Writer - Remote **Job Description** The Senior Proposal ... products, and services to support Prime's sales objectives. The Senior Proposal Writer leads all aspects of...to their job, and comply with all applicable legal, regulatory , and contractual requirements and internal policies and procedures.… more
- J&J Family of Companies (West Chester, PA)
- …of America **Job Description:** We are searching for the best talent for a ** Senior Medical Writer , Scientific Operations,** to join our MedTech Team. Remote ... their journey to wellness. Learn more at https://www.jnj.com/medtech **Purpose:** The Senior Medical Writer , Scientific Operations provides oversite and… more
- Stryker (Lansing, MI)
- Stryker is hiring a ** Senior Technical Writer , QMS - Product Security** ! In this role, you will be responsible for creating, reviewing, and maintaining ... high-quality documentation that complies with regulatory requirements and industry standards. You will translate complex...**What you will do:** + **Role Focus** : Technical Writer specializing in Quality Management Systems (QMS) for medical… more
- System One (Cleveland, OH)
- Job Title: Director / Senior Director Medical Writer Location: CST or EST candidates willing to work EST Type: Direct Hire Compensation: $165000 - $250000 ... annually Contractor Work Model: Remote As a Director or Senior Director, Medical Writer you will be responsible for document creation across clinical development… more
- Regeneron Pharmaceuticals (Armonk, NY)
- The Senior Medical Writer (SMW) works with team members and independently to write the content of clinical documents that may include CSRs, protocols, ICFs, ... variety of therapeutic areas. Opportunities to contribute to other regulatory documents may be provided. The SMW tracks their...to help ensure appropriate content for inclusion. **As a Senior Medical Writer , a typical day may… more
- IQVIA (Durham, NC)
- …bonne maitrise des outils informatiques. **Job Overview:** Acts as Lead Medical Writer on most types of writing projects. Prepares assigned documents in accordance ... customer requirements as well as to the agreed timelines. Performs Senior Review of straightforward medical writing deliverables. Negotiates timelines and… more
- Stryker (Portage, MI)
- Stryker is hiring a ** Senior Technical Writer ** in **Portage, MI** to support our **Instruments Divisions** ! In this role, you will support product development ... for an entire business unit according to user needs and regulatory requirements for domestic and international customers. + Interface cross-functionally within… more
- Actalent (Santa Clara, CA)
- Job Title: Technical Writer Job Description Collaborate with various teams to capture technical information and transcribe it into clear documentation for internal ... design change orders. + Provide oversight on proper documentation for regulatory submissions. Essential Skills + Medical device experience and understanding of… more
- SAIC (Washington, DC)
- **Description** **Job Title: FAA -** Senior Technical Writer /Editor - UAS Integration Office ** Sr . Technical Writer /Editor** Applies in-depth knowledge ... of performing technical writing functions with respect to FAA aviation regulatory documentation or related disciplines. Bachelor's Degree may be waived with… more
- Nanobiosym, Inc. (Cambridge, MA)
- …a PhD or Master's degree in a science discipline, and prior experience as a senior editor or lead writer for leading scientific journals, magazines, or research ... Cambridge, MA, USA | Contract Job Title: Scientific Writer (Onsite Consultant)Location: Cambridge, MA About the Role: We are seeking an experienced Scientific … more
- ERCOT (Austin, TX)
- …the Public Information Request apparatus, using research and knowledge of regulatory and industry requirements to determine appropriate responses + Explain ERCOT ... for publication, ensuring appropriate brand is reflected in all visual communication Level Senior /Lead - Above + Serves as a Subject Matter Expert providing guidance… more
- CVS Health (Bismarck, ND)
- …+ Familiarity with benefit terminology. + General understanding of compliance and regulatory issues, including ERISA, HIPAA, ACA, and COBRA. + Strong organizational ... skills with the ability to manage time efficiently and consistently meet or exceed deadlines. + Prior insurance industry and benefits experience preferred. **Education** + High school diploma, GED, or equivalent work experience preferred. **Anticipated Weekly… more
- Actalent (Philadelphia, PA)
- Lead Medical Writer Job Description We are seeking a highly experienced Senior Medical Writer to join our team and contribute significantly to our growing ... workload. This role involves writing specific clinical and regulatory documents while managing the process efficiently, ensuring successful cross-functional… more
- Grifols Shared Services North America, Inc (San Diego, CA)
- …than 110 countries and regions. Grifols Diagnostic Solution is seeking an Instrument Documentation Writer in San Diego, CA. This role will be reporting to the ... Senior Manager, Verification and Validation. This position will provide...development. + Ensure compliance of labeling with all applicable regulatory /QSR requirements. + Create and edit documentation in compliance… more
