- 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
- ThermoFisher Scientific (Greenville, NC)
- …and regional regulations and codes of practice. In addition, the Senior Medical Writer will provide high-quality medical and scientific writing from planning and ... and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need.… 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
- IQVIA (Durham, NC)
- We are seeking a ** Scientific Writer - Vaccines** to join Q2 Solutions, IQVIA's laboratory business as a remote position. We hire passionate innovators who drive ... we transform and accelerate research and development. As a Scientific Writer - Vaccines, you will be...senior support, and staying updated on medical/technical writing and regulatory knowledge, including GCP and advances in drug development.… 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
- AbbVie (Chicago, IL)
- …clinical documents and clinical documents for regulatory submissions. Provides scientific publications or clinical regulatory document support and ... knowledge of US and international regulations, requirements, and guidance associated with scientific publications or clinical regulatory document preparation… 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
- Randstad US (Marietta, PA)
- technical writer - first shift. + marietta , pennsylvania + posted 2 days ago **job details** summary + $42 - $44.01 per hour + contract + bachelor degree + category ... + reference48863 job details job summary: - Serve as a Technical Writer dedicated to authoring, revising and improving documents within manufacturing. (Business… 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
- Randstad US (Marietta, PA)
- technical writer . + marietta , pennsylvania + posted 2 days ago **job details** summary + $30.76 - $42.76 per hour + contract + bachelor degree + category computer ... and mathematical occupations + reference1065043 job details job summary: A Technical Writer is needed for a leading pharmaceutical manufacturer in the Marietta, PA… 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)
- …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