- Merck & Co. (Rahway, NJ)
- …disclosure, and data sharing with external researchers. - The Specialist (Disclosure Medical Writer ) will be primarily responsible for preparing clinical study ... writing, familiarity with clinical research documents preferred.Experience in medical publications or regulatory product labeling.Preferred Experience and… 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
- ThermoFisher Scientific (Allentown, PA)
- …and perspectives are valued. **What will you be doing in this Senior Medical Writer role focused on Promotional Review work?** Provides tailored high-level ... national and regional regulations and codes of practice. In addition, the Senior Medical Writer will provide high-quality medical and scientific writing… more
- AbbVie (Remote, OR)
- …LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description Summary The Senior Medical Writer is responsible for providing medical writing, ... that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a...required or in a related area such as quality, regulatory , publications, clinical research, or product support/R&D. 3 years… more
- AbbVie (Mettawa, IL)
- …Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description Summary The Principal Medical Writer is responsible for providing writing support and ... that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a...required or in a related area such as quality, regulatory , publications, clinical research, or product support/R&D. 2 years… more
- Fallon Health (Worcester, MA)
- …management processes and procedures + Ability to review and interpret regulatory -governed documents and medical terminology, and condense said language ... **Overview** **The Prior Authorization Letter Writer position works M - F 8 am...criteria, MassHealth, and CMS guidelines to ensure NQCA and regulatory compliance. **Responsibilities** **Primary Job Responsibilities:** + Utilizing knowledge… more
- Flywheel Partners (Boston, MA)
- …collaborators, effective communicators, and detail-oriented professionals. We are searching for a medical writer (aka scientific writer , content developer) ... Attend scheduled status calls and client review meetings with Medical , Marketing, Sales, Legal, and Regulatory +...and trust + Professional Development + Learn the Senior Medical Writer and Medical Manager… more
- Pfizer (Boston, MA)
- **ROLE SUMMARY** + The Medical Writer (Senior Manager/Associate Director) creates documents pertaining to clinical studies and regulatory interactions, ... regulations and industry standards, new technology, and new processes that impact Medical Writing. + Proficiency with global regulatory guidance (especially ICH,… more
- Merck (Columbus, OH)
- …document disclosure, and data sharing with external researchers. The Specialist (Disclosure Medical Writer ) will be primarily responsible for preparing clinical ... writing, familiarity with clinical research documents preferred. + Experience in medical publications or regulatory product labeling. **Preferred Experience and… more
- Publicis Groupe (Philadelphia, PA)
- …and championing the science that fuels medical impact. **Overview** The Senior Medical Writer will be responsible for the conception and execution of ... New York City // Philadelphia // Chicago and many remote employees. We want our talent to be comfortable...influence goes beyond the agency too-clients, stakeholders, and the Medical /Legal/ Regulatory review (MLR) team look to us… more
- Danaher Corporation (Miami, FL)
- …laboratory science and patient care? Then read on! We are currently seeking a Medical and Scientific Writer who will be responsible for supporting our global ... Medical and Scientific Affairs team. This role will work...plus if you also possess previous experience in: + Regulatory submissions + Market access research understanding At Beckman… more
- Elevance Health (Denver, CO)
- …in-office) with PulsePoint sites used for collaboration, community, and connection. This includes remote work and 1-2 days in office per week. Candidates must reside ... each way of a relevant Elevance Health location. The **Provider Communication Writer Sr** is responsible for providing writing support for the development and… more
- MD Anderson Cancer Center (Houston, TX)
- …the public. **SUMMARY** Writes, edits and coordinates production of highly technical medical material. Retrieves data from databases and other internal and external ... patient education/materials, IRB forms. Works collaboratively with research nurse manager and regulatory staff to develop or coordinate the development of the study… more
- Pfizer (Sanford, NC)
- …Drug Substance and Drug products to facilities around the globe. This Technical Writer position is designed to write, or support the development of, various ... to work additional times to support emergency manufacturing needs (either onsite or remote ) Work Location Assignment: On Premise The annual base salary for this… more
- CH Robinson (Atlanta, GA)
- …the world's largest logistics platforms and we're looking for our next **Customs Entry Writer ** . Is that you? You'll be responsible for the accurate and timely ... expert in our systems and processes and provide on-going regulatory training. Many of our successful Customs Entry Writers...creativity and driving impactful results. With the flexibility for remote work 3 days a week, this role strikes… more
- Dairyland Power Cooperative (La Crosse, WI)
- …process changes or introduce latest items. 6. Prepare the organization for regulatory changes that will require changing process or tooling; collaborate with Safety, ... of a wide array of tools, including utility specific applications + Technical Writer + Excellent verbal and written communication skills with the ability to… more
- PSEG (Salem County, NJ)
- …location categories: onsite roles, hybrid roles that are a blend of onsite and remote work, remote local roles that are primarily home-based but require some ... of purpose-driven in-person interaction and living within a commutable distance, and remote non-local roles that can be effectively performed remotely with the… more
- Takeda Pharmaceuticals (Columbus, OH)
- …collaboration. You will also contribute to therapeutic area project teams as the medical writing expert for regulatory submission documents. Collaborate with all ... Takeda regions to ensure a medical writing regulatory document strategy is created...projects, process, and standards). As required, serves as lead writer for important regulatory response documents and… more
- Takeda Pharmaceuticals (Columbus, OH)
- …**Job Description** **About the role:** **Associate Director, Nonclinical Regulatory Writing and Submission Support,** **_Oncology and Marketed Products_** ... work? Join us as an _Associate Director - Nonclinical Regulatory Writer_ _and Submission Support_ reporting to the Nonclinical...(8am - 5pm ET)._ + _Although this position is remote , occasional face-to-face meetings may be important to attend… more
- Dana-Farber Cancer Institute (Brookline, MA)
- …positive, results-oriented culture founded on open communication. This position is considered remote , 0-1 days onsite at 10 Brookline Place, Brookline, MA each week. ... physician/researchers, and we work with amazing partners, including other Harvard Medical School-affiliated hospitals. + Lead strategic content efforts to solicit… more
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