- Houston Methodist (Houston, TX)
- At Houston Methodist, the Scientific Writer position is responsible for performing a variety of tasks including preparing laboratory and clinical studies and ... agency requirements. + Prepares moderately complex documents and sections of regulatory submissions and contributes scientific knowledge and analytical skills… more
- University of Miami (Miami, FL)
- …of Miami/UHealth Department of SCCC has an exciting opportunity for a Full Time Scientific Writer to work at the UHealth Medical Campus. The Scientific ... clarity, consistency, and compliance with applicable submission requirements. + Reviews document language for scientific and medical accuracy; suggests… more
- Kelly Services (Sunnyvale, CA)
- Kelly(R) Science & Clinical is currently recruiting for a Technical Writer for a 6-month contract opportunity with a leading molecular diagnostics company at their ... Sunnyvale, CA. If you are driven by the prospect of translating cutting-edge scientific discoveries into tangible advancements and are poised to advance your career,… more
- MD Anderson Cancer Center (Houston, TX)
- …a submission-ready document . Writing for technical audiences Writes and edits scientific research proposals, grants, and reports at the direction of the research ... patient education/materials, IRB forms. Works collaboratively with research nurse manager and regulatory staff to develop or coordinate the development of the study… more
- McLaren Health Care (Detroit, MI)
- **Position Summary:** **The Scientific /Medical Writer ** plays a critical role in the development and execution of Karmanos Cancer Institute (KCI) oncology ... (IRB)/ regulatory authorities to ensure accuracy and compliance. 4. Document Management: Maintain and update protocol documentation, ensuring all versions are… more
- Kelly Services (Deerfield, IL)
- …Responsibilities:** + With oversight, develops high quality clinical documents ensuring scientific excellence and regulatory compliance. + The development ... & Clinical** **(R)** is seeking an experienced Sr. Medical Writer for a short term contract with a Global...writing skills. + 5 years of on-the-job experience in scientific /medical writing eg, clinical trial and regulatory … more
- Publicis Groupe (Philadelphia, PA)
- …inspire HCPs, and ultimately lead to improved patient outcomes. Given our scientific and medical talent, powerful data warehouse and creative digital solutions, we ... current clients are excited about a more modern medical communications and scientific exchange that delivers a future-forward customer experience and meets the… more
- Merck (Boston, MA)
- …the Translational Medicine clinical writing portfolio. **The Associate Principal Medical Writer :** + Independently leads and authors clinical regulatory ... **Job Description** The Associate Principal Medical Writer is responsible for leading medical writing deliverables...submission, etc.) across all therapeutic areas per company and regulatory requirements. + Demonstrates expertise in document … more
- Kelly Services (Sunnyvale, CA)
- **Technical Writer ** **Shift** : M-F, standard working hours **Location** : Sunnyvale, CA (hybrid) **Pay** : $50-$60/hr **6 month contract role** **Overview** : The ... Technical Writer is responsible for writing, editing, formatting, and managing...in vitro diagnostic Xpert tests and GeneXpert instrument systems. Document types include Instructions for Use, Quick Reference Instructions,… more
- System One (Bothell, WA)
- …+ Deviation Management: + Collaborate with laboratory staff, quality assurance, and regulatory affairs teams to document and assess deviations in laboratory ... Job Title: Technical Writer Location: Bothell, WA Hours/Schedule: M-F, Normal business...stakeholders when assessing the impacts of laboratory deviations. + Regulatory Compliance: + Stay up to date with industry… more
- ManpowerGroup (Marietta, PA)
- …practices. + **Quality & Compliance:** + Ensure documents meet quality and regulatory standards. + Manage document formatting, revisions, and change requests. ... **Biopharmaceutical Technical Writer ** **Marietta, PA** **Pay:$78,000-$85,000 annual** Visa Sponsorship? Not offered Corp-to-Corp? Not eligible Must be a US Citizen… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …advanced knowledge of BLA/MAA submissions, working knowledge and experience in document management systems, relevant therapeutic areas, regulatory requirements, ... science and technology. With more than 120 years of scientific expertise and a presence in more than 20...and immune disorders. **Job Summary:** The Associate Director of Regulatory Writing is a key role responsible for producing… more
- J&J Family of Companies (Columbus, OH)
- …Writing interdependencies between all major documents of electronic Common Technical Document (eCTD) is required. + Experience conducting Regulatory Medical ... Director, Regulatory Medical Writing (1 of 4) - 2406211847W... Medical Writing (RegMW) is a highly experienced medical writer and influential leader with strategic responsibilities as it… more
- J&J Family of Companies (Columbus, OH)
- …plans, regulatory responses, and briefing documents. + Lead cross-functional document planning and review meetings. Interact with peer writers and colleagues ... Senior Analyst, Immunology Regulatory Medical Writing - 2306143143W **Description** At Johnson...groups. + Coach or mentor more junior writers on document planning, processes, content, and provide peer review as… more
- Gilead Sciences, Inc. (Foster City, CA)
- …authorities, including system, processes and requirements. + In-depth knowledge of regulatory document requirements and guidelines relevant to assigned products, ... development and commercial product lifecycle management and contributes strategic, expert input into scientific and regulatory content that is used for a variety… more
- ManpowerGroup (Deerfield, IL)
- …Responsibilities: * With oversight, develops high quality clinical documents ensuring scientific excellence and regulatory compliance. The development process ... client in pharmaceutical Industry is seeking a Sr Medical Writer to join their team. The ideal candidate will...excellent writing skills. 5 years of on-the-job experience in scientific /medical writing (eg, clinical trial and regulatory … more
- BeiGene (San Mateo, CA)
- …clinical regulatory documents that conform to domestic and/or international regulatory submission and internal document standards, while meeting project ... INDs, MAAs, and NDAs is a plus + The technical/ scientific ability to critically analyze, synthesize, and present complex...+ 7+ years of relevant industry experience as a regulatory medical writer with a BA/BS degree.… more
- Amentum (Richmond, VA)
- …as a classroom instructor, exercise observer/controller, workshop facilitator, and technical writer for Amentum's ROK CWMD Readiness Project. The position is ... forces on technical topics, principles, theories, and concepts of varying scientific complexity with limited background knowledge + 10+ years' experience managing… more