- Citigroup (New York, NY)
- Serves as a Regulatory Response and Oversight Regulatory Response Writer responsible for the promotion, support, monitoring and reporting related to Citi's ... and programs to prevent violations of law, rule, or regulation and deliver regulatory responses. In addition, engages with the product and function coverage teams,… more
- AbbVie (Barceloneta, PR)
- …@abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description The Senior Investigator Writer is responsible for providing quality assurance ... medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's… more
- Abbott (Alameda, CA)
- …spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues ... improve people's health. We're always looking towards the future, anticipating changes in medical science and technology. **Working at Abbott** At Abbott, you can do… 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 ... ESSENTIAL FUNCTIONS** + Prepares moderately complex documents and sections of regulatory submissions and contributes scientific knowledge and analytical skills to… more
- Robert Half The Creative Group (Denver, CO)
- Description Robert Half Marketing & Creative is seeking a skilled Technical Writer with experience in both software documentation and the agriculture industry to ... and usability. + Stay updated on industry trends, software updates, and regulatory requirements to ensure documentation remains relevant and up-to-date. + Assist in… more
- STERIS (Plymouth, MN)
- Senior Technical Writer & Editor Req ID: 41992 Job Category: Engineering Plymouth, MN, US, 55441 Description: At STERIS, we help our Customers create a healthier ... with minimal supervision on routine activities and under general supervision of Senior Staff on non-routine activities. Management Axis: 1. Has no direct reports.… more
- Wells Fargo (Charlotte, NC)
- **About this role:** We're looking for a Senior Content Designer to write for Fargo, our AI-powered virtual assistant. Working in a fast-paced, collaborative team of ... all applicable risk programs (Credit, Market, Financial Crimes, Operational, Regulatory Compliance), which includes effectively following and adhering to applicable… more
- CVS Health (Tampa, FL)
- …and affordable. Position Summary Under general supervision, drafts, reviews, and edits medical , dental and vision plan documents. This position will support plan ... industry and benefit experience is preferred. + Knowledge and experience in medical , dental and vision benefits. + Knowledge and experience in benefit terminology.… more
- University of Miami (Miami, FL)
- …The Sylvester Comprehensive Cancer Center has a great opportunity for a Scientific Writer . The Writer analyzes, simplifies, writes, and designs well - organized, ... best meet the needs of both internal and external audiences. Further, the Writer (N) gathers facts, figures, personal stories, and evidence of the University's… more
- Truist (Charlotte, NC)
- …databases + Obtain a solid understanding of all compliance and regulatory requirements as it pertains to RFP submissions **Qualifications** **Required ... by the division of Truist offering the position. Truist offers medical , dental, vision, life insurance, disability, accidental death and dismemberment, tax-preferred… more
- Novo Nordisk (Lexington, MA)
- …aligned with reporting requirements and company objectives. Relationships Reports to Senior Nonclinical Writer , Program Development. This position may be ... ready to make a difference? The Position The nonclinical writer will be a key member of the Program...nonclinical groups to manage all aspects of preparation for regulatory documents and scientific reports according to company guidelines… more
- IQVIA (Durham, NC)
- …to customer comments with senior support, and staying updated on medical /technical writing and regulatory knowledge, including GCP and advances in drug ... We are seeking a **Scientific Writer - Vaccines** to join Q2 Solutions, IQVIA's...project needs, tracking timelines and implementing customer requests, keeping manager/ senior staff abreast of progress on tasks and any… more
- System One (Rockville, MD)
- …/ Friday remote and Tuesday, Wednesday, Thursday on-site. Our client is currently hiring a Senior Science Writer to focus on mental health and substance use. The ... a Direct Hire position open for a Sr Scientific Writer . If you or anyone you know is...collaborating with subject matter experts, and reviewing legislative and regulatory guidance + Assess and incorporate reviewer feedback +… more
- AbbVie (Barceloneta, PR)
- …Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description The Senior Investigator Writer Leader is responsible for the writing and/or ... medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's… more
- Belcan (Thousand Oaks, CA)
- …quality, reliability engineering, domain experts from commercial, clinical, molecular research, medical sciences, regulatory , drug substance and drug product ... Technical Writer - Life Science Job Number: 347583 Category:...and Lifecyle Management group in Thousand Oaks, CA, supporting senior staff in design, characterization, and qualification of combination… more
- Alaka'ina Foundation Family of Companies (Frederick, MD)
- …Social Science Support - Positions may include: Biostatistician; Clinical Data Manager/ Regulatory Writer ; Quality Assurance Officer; Regulatory Scientist; ... Regulatory , Clinical, and Technical Clinical Trial support Location...Technical Writer ; Program Manager; Biomedical Science Writer ; Principal Investigator. + Medical Services -… more
- Publicis Groupe (New York, NY)
- …+ Provide guidance to PM and Account teams as they prepare projects for Medical Legal Regulatory (MLR) review + Submit completed materials to the client, ... Wellness has provided consumer and professional marketing, strategic consulting, and medical education to pharmaceutical and wellness brands. Our mission is to… more
- Boehringer Ingelheim (Ridgefield, CT)
- …clinical development and achieve regulatory approvals and reimbursable medicines. Senior CPL provides continuous medical benefit and risk oversight for ... continuous risk/benefit assessment. + Authors Investigator Brochures (with support from the Medical Writer and other contributors), Clinical Development Plans or… more
- Stanford Health Care (Emeryville, CA)
- …or he has contributed and been recognized as a co-author or acknowledged as a medical writer , or an example of "enduring materials" in other media. Participation ... best is waiting to be discovered. Day - 08 Hour (United States of America) Senior Director, Quality - Cancer DSL Location: Palo Alto, CA Reporting to and partnering… more
- BeiGene (Emeryville, CA)
- …be responsible for creating and maintaining Medical Affairs slide decks. The Medical Writer will collaborate with Medical Affairs stakeholders to create ... to BeiGene SOPs, work instructions, and quality standards + Apply legal, regulatory , and compliance requirements to all Medical Affairs activities **Supervisory… more