- Merck & Co. (North Wales, PA)
- …as the lead clinical scientist on the clinical trial team.Collaborates with the Medical Writer on clinical/scientific and regulatory documents.Partners with ... design during study start up (eg, database set up)Lead medical monitoring team in review and interpretation of clinical...by site or organization, with Friday designated as a remote -working day, unless business critical tasks require an on-site… more
- System One (Baxley, GA)
- System One is seeking a Technical Writer for a fully remote , 6-month contract position. This role will support our client in the nuclear industry by assisting ... with procedure updates and enhancements. Technical Writer Responsibilities: + Review and analyze procedure change assignments, typically provided as redlined PDF… more
- Actalent (Gaithersburg, MD)
- Pharmaceutical company seeking an experienced Medical Writer with both clinical and regulatory writing expertise. Applicants must be located on the East ... Coast. Position Summary: The Medical Writer will work with the clinical and regulatory teams to prepare regulatory submissions, protocols including… more
- Actalent (Gaithersburg, MD)
- Pharmaceutical company seeking an experienced Medical Writer with both clinical and regulatory writing expertise. **Applicants must be located on the East ... Qualifications: + Bachelor's Degree required; advanced degree in a relevant scientific/clinical/ regulatory field preferred + 8+ years Medical Writing experience… 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
- Adecco US, Inc. (Bridgewater, NJ)
- …onsite at Bridgewater, NJ and few days for the first few months) Duties The CMC Regulatory Technical Writer II authors high quality Module 2 and 3 regulatory ... such as white papers, position papers, and briefing book. In parallel, the technical writer could help support non regulatory writing projects such as SOP and… more
- ThermoFisher Scientific (Juneau, AK)
- **Work Schedule** Standard (Mon-Fri) **Environmental Conditions** Office **Job Description** **Senior Medical Writer (North America) (FSP; Remote )** At ... Medical Writing FSP Team! This would be a remote role working from any location in North America....in North America. We are looking for a Senior Medical Writer to be dedicated to a… 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
- Pfizer (Groton, CT)
- **JOB 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
- 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
- IQVIA (Durham, NC)
- …responding to customer comments with senior support, and staying updated on medical /technical writing and regulatory knowledge, including GCP and advances in ... We are seeking a **Scientific Writer - Vaccines** to join Q2 Solutions, IQVIA's...to join Q2 Solutions, IQVIA's laboratory business as a remote position. We hire passionate innovators who drive healthcare… 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
- 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
- Wells Fargo (San Francisco, CA)
- …accessibility (ADA) and search engine optimization (SEO) + Comfortable working with both remote and in person teammates and in an Agile environment + A storyteller ... all applicable risk programs (Credit, Market, Financial Crimes, Operational, Regulatory Compliance), which includes effectively following and adhering to applicable… 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
- Edwards Lifesciences (St. Paul, MN)
- …scientific experience **What else we look for (Preferred)** : + Experience as a medical writer for a medical device company, cardiovascular medical ... patients around the world. From design to production, our Regulatory Affairs teams help guide our innovative technologies through...and be part of our inspiring journey. The Manager, Medical Writing will provide guidance, develop, and lead … 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
- 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 (Raritan, 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
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