- 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
- AbbVie (North 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
- Medical Mutual of Ohio (OH)
- …financial data, understand trend and formulate recommendations on coverage under the medical plan. **Sr Healthcare Analyst- Policy Writer ** **Education and ... Founded in 1934, Medical Mutual is the oldest and one of...organizations. **_This position has the option to work fully remote ; Cleveland, Ohio area residents preferred._** **Responsibilities** **Healthcare Analyst-… more
- Cook Medical (West Lafayette, IN)
- …development. CRI is currently accepting applications for a Scientific Communications Scientist (ie, Medical Writer ) to become a part of our growing Scientific ... companies. This position is eligible to be hybrid or remote . Responsibilities + Write and direct the preparation of...Provide status updates on deliverables to management; + Understand medical writing and regulatory standards and practices;… 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
- NANA Regional Corporation (Oak Ridge, TN)
- …15,000 Inupiat shareholders, a group of Alaska natives from one of the most remote and harshest environments in the United States. **For our shareholders** , AIS ... material testing, metrology, procurement, radiography,and weld inspection. + The writer is responsible for complying with Y15-232, Technical Procedure Process,… more
- Robert Half The Creative Group (Milwaukee, WI)
- Description We are offering an opportunity to join our team as a Technical Writer in the healthcare industry. This remote role is based out of Milwaukee, ... Wisconsin and involves developing high-quality clinical documents to support regulatory submissions for our products. The role requires an understanding of global … more
- RELX INC (Horsham, PA)
- UX Writer & Conversation Designer About our Team At LexisNexis Intellectual Property (LNIP), we believe that whenever a person works on a patent and understands the ... to better humankind. About the Role As a UX Writer & Conversation Designer at LNIP, you'll play a...work/life balance across the organization, with various flexible and remote working options available to employees. Working for you… more
- AECOM (Sacramento, CA)
- …deliver a better world. Join us. **Job Description** **AECOM** is seeking a **Technical Writer ** to be based in Sacramento, CA **.** **JOB SUMMARY:** The technical ... writer position will be responsible for editing and formatting...prepare documents for audience-targeted readability (eg, general public, client-specific, regulatory authorities) + Knowledge and basic experience in 508… 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
- MD Anderson Cancer Center (Houston, TX)
- …MMO clinical research team. Protocols need to be of high quality for internal regulatory review (SRC, IND office, and IRB), and appropriate for IND submissions and ... investigators and MMO clinical research team in addressing responses to internal regulatory and external reviewers in a timely fashion. **Collaboration with Other… more
- Organon & Co. (Lansdale, PA)
- …Excel, e-mail, and online meeting tool skills. + At least 12 years of regulatory medical writing experience is required. + Experience as lead writer ... submissions required. + At least 12 years of regulatory medical writing experience is required. +... writing experience is required. + Experience as lead writer for key documents included in major US/EU and/or… more
- Boehringer Ingelheim (Ridgefield, CT)
- …continuous risk/benefit assessment. + Authors Investigator Brochures (with support from the Medical Writer and other contributors), Clinical Development Plans or ... cross-functional evidence team (Clinical Operations, Biostatistics, Translational Medicine, Pharmacovigilance, Regulatory , Medical Affairs, Market Access, Epidemiology, RWE… more
- Boehringer Ingelheim (Ridgefield, CT)
- …by Medicine Excellence Project 2020. The CDOL will collaborate with other functions ( Medical Writer , Study Physician, Clinical Program Leader, PSTAT and PDM) to ... technologies in healthcare + Advanced knowledge of existing and emerging global regulatory , ethical and compliance requirements for clinical research. + Proven track… more
- J&J Family of Companies (Columbus, OH)
- …cardiovascular and metabolic diseases. Within Integrated Data Analytics & Reporting (IDAR), the Regulatory Medical Writing team are recruiting for a **Principal ... Principal Medical Writing Scientist - Immunology - 2306143143W **Description**...Spain, Italy, Poland, Bulgaria or Switzerland), or other countries. Remote work options may be considered on a case-by-case… more
- J&J Family of Companies (Columbus, OH)
- …cardiovascular and metabolic diseases. Within Integrated Data Analytics & Reporting (IDAR), the Regulatory Medical Writing team are recruiting for a **Principal ... Principal Medical Writing Scientist, Oncology Late Development (1 of...Raritan, NJ, Titusville, NJ, or Canada), or other countries. Remote work options may be considered on a case-by-case… more
- J&J Family of Companies (Titusville, NJ)
- …cardiovascular and metabolic diseases. Within Integrated Data Analytics & Reporting (IDAR), the Regulatory Medical Writing team are recruiting for a **Principal ... Principal Medical Writing Scientist, Oncology - 2306144391W **Description** **Principal...Raritan, NJ, Titusville, NJ, or Canada), or other countries. Remote work options may be considered on a case-by-case… more
- Organon & Co. (Washington, DC)
- …external stakeholders to draft formal comments related to federal and state regulatory action. Develop public policy positions and cover policy issues consistent ... and Policy Officer, develop policy proposals to improve the regulatory and statutory environment relevant to the business operations...for owning projects and driving them to completion. Skilled writer capable of adapting to a range of purposes,… more
- AECOM (Buffalo, NY)
- …staff and leading multi-discipline project design teams. + Interface with client and regulatory agencies and play a major role on presentations to existing or ... experience + Strong communication skills in coordinating with clients, sub-consultants, regulatory agencies, and members of the public to accomplish assigned… more
- Pfizer (Boulder, CO)
- …to leverage digital diagraming tools and communicate technical requirements in a remote setting. + Strong understanding of Agile, SDCL, CI/CD, DevOps, GitOps, and ... have experience working in Jira and Confluence, and be a strong writer , contributing to engineering team documentation/playbooks. + Prioritizes excellence in data… more
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