- Novo Nordisk (Plainsboro, NJ)
- …development and regulatory requirements of a clinical program. The Principal Medical Writer will provide high level strategic input into development plans, ... study designs, and regulatory submissions. Relationships The Principal Medical Writer reports to a Director of Medical Writing. The Principal Medical … more
- BeiGene (San Mateo, CA)
- …and PowerPoint. Education/Experience Required: + 7+ years of relevant industry experience as a regulatory medical writer with a BA/BS degree. All qualified ... project timelines and to oversee these activities in more junior medical writers. Clinical regulatory documents include, but are not limited to study reports,… more
- AbbVie (Chicago, IL)
- …Pharmaceutical Writing. + Minimum of 4 years of relevant industry experience in medical / regulatory writing in the healthcare industry or academia required, or in ... that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a...Facebook, Instagram, YouTube and LinkedIn. Job Description The Principal Writer (PW) is responsible for providing RA strategic document… more
- Abbott (Santa Clara, CA)
- …from routine fingersticks. **The Opportunity** The function of a **Senior Medical Writer /Project Manager** supporting our Vascular Clinical Evaluation Products ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
- Takeda Pharmaceuticals (Columbus, OH)
- …Medical Writing Team Lead, the Principal Medical Writer guides medical writing activities for key clinical and regulatory documents and regulatory ... therapies to patients worldwide. Join Takeda as a Principal Medical Writer where you will working across...for key clinical and regulatory documents and regulatory submissions; guides medical writing document preparation,… more
- Novo Nordisk (Plainsboro, NJ)
- …a living. Are you ready to make a difference? The Position The Senior Medical Writer works closely with cross-functional project teams to manage preparation of ... requirements of a clinical program. Relationships The Senior Medical Writer reports to a Director of...years of relevant experience + Minimum of 5 years clinical/ regulatory medical writing experience in a pharmaceutical,… more
- MicroVention, Inc. (Aliso Viejo, CA)
- **12251BR** **Title:** Sr. Medical Writer (PhD or MD) **Job Description:** **INNOVATION STARTS WITH YOU** Are you interested in working for an organization that ... (R) **TERUMO** has to offer. **Position Overview** The Sr. Medical Writer / Medical Writer ...documents and scientific presentations in cooperation with the Clinical, Medical , & Regulatory Affairs Teams, KOLs and… more
- System One (Bellevue, WA)
- System One, is seeking to contract with a motivated Nuclear Power Plant Procedure Writer to support our client in Bellevue, WA. This is a 12 month remote contract ... outside organizations working on procedure development. + Nuclear Operations Procedure Writer will focus on development of administrative and operating procedures.… more
- Kelly Services (Deerfield, IL)
- **Kelly Science & Clinical** **(R)** is seeking an experienced Sr. Medical Writer for a short term contract with a Global Biotech Company. **Job Title: Sr. ... Medical Writer Specialist in Worldwide ...Medical Writer Specialist in Worldwide Medical Advanced Surgery**...writing skills. + 5 years of on-the-job experience in scientific/ medical writing eg, clinical trial and regulatory … more
- Integra LifeSciences (Princeton, NJ)
- …in med device/pharmaceutical/biotech industry, with at least 5 years of experience as medical writer . + Expertise with software and templates commonly used in ... create quality system documentation and responses in support of regulatory compliance correspondence. The Quality Compliance Technical Writer... regulatory medical writing (eg, MS-Word, Excel, PowerPoint,… more
- BWX Technologies, Inc. (Erwin, TN)
- …the safe operation of equipment, procedure flow and usability, and adherence to regulatory requirements and writer 's guidelines. + Interface with Subject Matter ... of Energy and NASA facilities. BWXT's technology is driving advances in medical radioisotope production in North America and microreactors for various defense and… more
- Pfizer (New York, NY)
- **ROLE SUMMARY** + The Medical Writer (Senior Manager/Associate Director) creates documents pertaining to clinical studies and regulatory interactions, ... industry standards, new technology, and new processes that impact Medical Writing. + Proficiency with global regulatory ...impact Medical Writing. + Proficiency with global regulatory guidance (especially ICH, FDA, and EMA) relevant to… more
- Salado Isolation Mining Contractors (Carlsbad, NM)
- Procedure Writer Department:PI-TR Procedures Location:Carlsbad, NM Be part of the nation-s only repository for the disposal of nuclear waste known as Transuranic ... candidate will obtain process specific training and follow the WIPP facility writer 's guide with respect to format, order, clarity, conciseness, style and… more
- Astellas Pharma (South San Francisco, CA)
- **Nonclinical Scientific Writer -Bioanalytics** Do you want to be part of an inclusive team that works to develop innovative therapies for patients? Every day, we are ... world. We are committed to turning innovative science into medical solutions that bring value and hope to patients...**The Role:** In this role as a nonclinical Bioanalytics writer in Astellas Gene Therapy (AGT) group, you will… 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
- Navarro Inc. (Oak Ridge, TN)
- …working with Department of Energy (DOE) proposals and a understanding of the regulatory and environmental landscape. The Senior Proposal Writer will be ... Navarro Research and Engineering is recruiting a Senior Proposal Writer in Oak Ridge, TN. Navarro Research & Engineering is an award-winning federal contractor… more
- Harvard University (Cambridge, MA)
- Details Title Scientific Writer /Project Manager (Research Associate) School Harvard Medical School Department/Area Department of Microbiology Position ... Description We are seeking a Scientific Writer /Project Manager (Research Associate) to provide communication support for...for the laboratory of Dr. Jonathan Abraham at Harvard Medical School. The Abraham lab uses methods in molecular… more
- Publicis Groupe (Philadelphia, PA)
- …to build a new way of educating and championing the science that fuels medical impact. **Job Description** This dedicated writer will be responsible for the ... and content. Our influence goes beyond the agency too-clients, stakeholders, and the Medical /Legal/ Regulatory review (MLR) team look to us for insights and… more
- Athena Global Advisors (Philadelphia, PA)
- …along the way. About the Position We're looking for an exceptional Writer with experience developing narratives and content for corporate communications clients. As ... a Writer at Athena supporting a Fortune-30 client, you will...industry. + Research: Conduct thorough research on industry trends, regulatory changes, technologies, and practices to ensure accuracy and… more
- KBR (Houston, TX)
- Title: LNG Technical Procedure Writer KBR Sustainable Technology Solutions (STS) provides holistic and value-added solutions across the entire asset life cycle. ... to optimize planned and operating assets. The LNG Technical Procedure Writer will develop Commissioning, Start-up, and Operations (CSO) technical documentation on… more