- Daiichi Sankyo, Inc. (Bernards, NJ)
- …science field preferred Experience Qualifications4 or More Years of experience as a medical writer with a graduate degree (Doctorate preferred) in a relevant ... diseases and immune disorders. Summary The Associate Director of Regulatory Writing is a key role responsible for producing...science field7 or More Years of experience as a medical writer with a Bachelor's degree in… more
- Actalent (Rockville, MD)
- …degree preferred. Additional Skills & Qualifications + 4-5 years of experience as a Medical Writer with regulatory submissions and CSR development background ... Job Title: Senior Medical Writer Job Description Responsibilities +...clinical product development, clinical research, clinical study design, biostatistics, medical terminology, research methodology, regulatory environment including… 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
- Humera (Maple Grove, MN)
- …Device Writer II, for our client based in Maple Grove, MN The Sr. Medical Writer on the Regulatory Clinical Evaluation team provides technical and ... Medical Writer II | Maple Grove,... Medical Writer II | Maple Grove, MN Medical...including clinical evaluation plan, PMS and PMCF plans, SSCPs, regulatory responses and other items + Evaluates and summarizes… more
- Regeneron Pharmaceuticals (Armonk, NY)
- …writing clinical documents for regulatory submissions. In this role, the Medical Writer will gain experience: + Drafting documents integral to clinical ... Regeneron is seeking a Medical Writer who is highly motivated...learn the skills needed to write a variety of regulatory documents and publications to support Regeneron's drug development… more
- Cordis (Irvine, CA)
- …people who keep saving lives. MedAlliance (Cordis) are currently seeking a **Technical Writer ** to join our Regulatory Affairs department, focusing on the ... for Use (IFUs), to support our product compliance and regulatory submissions. As a Technical Writer within...edit, and maintain clear and compliant IFUs and other regulatory documents for medical devices. + **Package… 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
- University of Miami (Miami, FL)
- …- Protocol Development Office (PDO) has an exciting opportunity for a Full Time Scientific Writer ( Medical Writer ) to work Remotely. CORE JOB SUMMARY The ... Scientific Writer analyzes scientific data and translates complex scientific concepts,...of clinical trials including protocol and ICF development, institutional regulatory submissions (Protocol Review and Monitoring Committee [PRMC] and… more
- Novo Nordisk (Lexington, MA)
- …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
- System One (Horsham, PA)
- Title: Medical Writer - Scientific Communications Location: Remote (or local to Horsham, PA) Salary: $160,000-$170,000 - FTE INSTAFF Benefits Group: Scientific ... Communications Leading Pharmaceutical Company located in NJ is hiring a Medical Writer - Scientific Communications w/ 5+ years industry experience. If you want… more
- Grifols Shared Services North America, Inc (Columbus, OH)
- …pharmacy, or related areas. Advanced degree (MS, PhD, or PharmD) preferred. ** Medical Writer 1:** Typically requires 5 years of pharmaceutical experience ... in clinical research/ regulatory medical writing. (If PhD, equivalency is...(If PhD, equivalency is 2 years of pharmaceutical experience.) ** Medical Writer 2:** Typically requires 8 years… more
- System One (San Rafael, CA)
- Job Order #: 329444 Title of Position: Medical Writer Location: San Rafael, CA Type: Contract Pay Rate: $50-$54/hr. W2 ONLY (NO STEM OPT CANDIDATES) Hybrid (1-2 ... days in office to align with company policy). The Contract Medical Writer applies advanced documentation preparation and document project management skills to… more
- Flywheel Partners (New York, NY)
- …effective communicators, and detail-oriented professionals. We are searching for a senior medical writer (aka scientific writer , content developer) with ... Lead scheduled status calls and client review meetings with Medical , Marketing, Sales, Legal, and Regulatory +...+ Learn the Flywheel pathways for advancement within the Medical Writer track, or other roles based… more
- Baptist Memorial (Memphis, TN)
- Summary The Scientific Writer will write, edit, and review manuscripts, grant proposals, research reports, and other scientific communications. Responsibilities ... developing project synopses, outlines, and complete scientific works. The Scientific Writer will ensure effective communication of analytic findings and perform… more
- J&J Family of Companies (Spring House, PA)
- …their potential. At Johnson & Johnson, we all belong. The Nonclinical Submissions Writer will prepare and review regulatory submission documents that summarize ... such as nonclinical safety, pharmacokinetic, and discovery biology project leaders, medical writers, global regulatory dossier leaders, and other subject… more
- Gilead Sciences, Inc. (Foster City, CA)
- …patients with life-threatening diseases. We are seeking a talented Scientific Publication Medical Writer with specialized experience in Viral Hepatitis & Liver ... our Headquarters in Foster City, CA., or Parsippany, NJ. **Scientific Publications Medical Writer :** + Collaborate with cross-functional teams to develop Viral… 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
- 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
- BAE Systems (Hill AFB, UT)
- **Job Description** BAE Systems is seeking a motivated, self-driven, Project Manager/Tech Writer for an exciting opportunity to support the Air Force's acquisition ... We are specifically looking for a detail-oriented and experienced Tech Writer to create and maintain comprehensive documentation for our aerospace engineering… 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
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