- Daiichi Sankyo, Inc. (Bernards, NJ)
- …by leveraging our world-class science and technology. With more than 125 years of scientific expertise and a presence in more than 20 countries, Daiichi Sankyo and ... diseases and immune disorders. Summary The Associate Director of Regulatory Writing is a key role responsible for producing...role will also contribute to strategic planning and provide scientific and strategic insights at the study team level.… more
- Merck & Co. (South San Francisco, CA)
- Job DescriptionWe are currently hiring an experienced document writer to join our team in South San Francisco, CA.The nonclinical pharmacology writing group prepares ... and related documents, managing author/management reviews, ensuring documents meet regulatory compliance requirements, and ensuring documents and document packages… more
- University of Miami (Miami, FL)
- …SCCC - 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 ...of clinical trials including protocol and ICF development, institutional regulatory submissions (Protocol Review and Monitoring Committee [PRMC] and… more
- Baptist Memorial (Memphis, TN)
- Summary The Scientific Writer will write, edit, and review manuscripts, grant proposals, research reports, and other scientific communications. ... Responsibilities include developing project synopses, outlines, and complete scientific works. The Scientific Writer will ensure effective communication of… more
- Houston Methodist (Houston, TX)
- The Scientific Writer at Houston Methodist, Department of Digital Health Innovation and Implementation Research position must have experience writing and editing ... science publications, and working with vendor and industry partners and executives. The scientific writer should have experience sourcing ways to present story… 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 ... audiences. The role requires a strong background in grant writing and scientific manuscript development. Please submit a cover letter with your online application.… more
- Houston Methodist (Houston, TX)
- At Houston Methodist, the Senior Scientific Writer is responsible for functioning as the mentor for junior staff with an extensive knowledge of both medical and ... ESSENTIAL FUNCTIONS** + Prepares moderately complex documents and sections of regulatory submissions and contributes scientific knowledge and analytical skills… more
- Bristol Myers Squibb (Summit, NJ)
- …group based in Summit, NJ and will be responsible for writing scientific documents including biomarker reports, regulatory documents (eg, non-clinical summaries, ... The Translational Medicine team supports the late-stage portfolio for regulatory , translational development and life cycle management. Translational Medicine… more
- University of Miami (Miami, FL)
- …experimental) for comprehensive analysis, assisting in the preparation of scientific manuscripts, presentations, and regulatory submissions. This list ... application templates for grant proposals. Formats substantive copy and scientific editing, proofreading, and finalizing documents as required and requested.… more
- Cardinal Health (Columbus, OH)
- …purpose of meeting objectives May act as mentor to less experienced colleagues The Regulatory Technical Writer (RTW) plays an important role in the Regulatory ... Affairs (GRA) team for all submission needs. The Writer in this position will develop documents required to...incorporating an understanding of the clinical development program, relevant scientific literature, and regulatory goals to drive… more
- Novo Nordisk (Lexington, MA)
- …provide high level strategic input into development plans, study designs, and regulatory submissions. Relationships The Principal Medical Writer reports to a ... Are you ready to make a difference? The Position The Principal Medical Writer is an expert in medical writing and performs work independently with minimal-to-no… more
- Grifols Shared Services North America, Inc (Bakersfield, CA)
- …clinical studies knowledge. Excellent knowledge of MS Office, Viso, ISI Writer , Reference Manager, and medical/ scientific search/retrieval tools. Excellent ... such as final Clinical Study Reports, abstracts, white paper reviews and regulatory agency submission documents on a given product or medical question across… more
- Robert Half The Creative Group (Irving, TX)
- Description Medical Writer - Contract - 40hrs/week - Hybrid Work Schedule Job Description: We are seeking a highly motivated and detail-oriented Medical Writer ... to our team of creative professionals. As a Medical Writer , you will play a pivotal role in producing...in producing high-quality content that communicates complex medical and scientific information to a broad audience. Your work will… more
- Novo Nordisk (Lexington, MA)
- …accuracy and consistency of clinical trial documents + A strong foundation in scientific knowledge enables the Medical Writer to understand and interpret ... Are you ready to make a difference? The Position The Senior Medical Writer works closely with cross-functional project teams to manage preparation of the written… more
- Idaho Division of Human Resources (Boise, ID)
- SENIOR HAZARDOUS WASTE PERMIT WRITER Posting Begin Date: 2025/02/12 Posting End Date: 2025/03/05 Category: Natural Resources Sub Category: Environmental Services ... Department of Environmental Quality (DEQ) is hiring a Senior Hazardous Waste Permit Writer - Scientist 4 for the Waste Management and Remediation Division for the… 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 is ... **TERUMO** has to offer. **Position Overview** The Sr. Medical Writer /Medical Writer will act as primary contact...job duties include: + Collaborating with the clinical & regulatory teams to write clinical documents for regulatory… more
- System One (San Rafael, CA)
- …following: + Medical writer in the pharmaceutical industry + Medical or scientific writing experience as a primary job responsibility Skill and Experience: + At ... Job Order #: 329444 Title of Position: Medical Writer Location: San Rafael, CA Type: Contract Pay...conducting clinical studies and reporting clinical study results for regulatory submissions and publications. RESPONSIBILITIES + Drafts and edits… more
- Humera (Maple Grove, MN)
- …Writer II, for our client based in Maple Grove, MN The Sr. Medical Writer on the Regulatory Clinical Evaluation team provides technical and strategic writing ... Medical Writer II | Maple Grove, MN Medical ...Experience in clinical study management and design, medical, or scientific writing, quality engineering, risk management is needed. Duties… more
- Publicis Groupe (Philadelphia, PA)
- …of the top 8 pharma companies on our roster. **Overview** The Senior Medical Writer will be responsible for the conception and execution of innovative print and ... be exactly who we are looking for. **ABOUT THE SCIENTIFIC TEAM** Here at the Medical team, we have...influence goes beyond the agency too-clients, stakeholders, and the Medical/Legal/ Regulatory review (MLR) team look to us for insights… more
- IQVIA (Durham, NC)
- …and competency) + Bachelor's degree required. Advanced degree in a relevant scientific /clinical/ regulatory field preferred. + At least 7 years medical writing ... The Associate Director, Principal Medical Writer is responsible for the development of clinical documents for submissions to regulatory authorities globally.… more
