- AbbVie (Chicago, IL)
- …. Job Description Responsible for leading and writing clinical and regulatory documents for drug and/or device development in support of company ... objectives. Responsibilities: * Responsible for leading and writing clinical and regulatory documents for drug and/or device development in support of company… more
- AbbVie (North Chicago, IL)
- …stakeholders & management; + interpreting statistical data to prepare written medical and scientific reports for regulatory bodies; + clinical regulatory ... + Serve as a lead on complex clinical & regulatory documents. + Work closely with the team(s) on...& Experience Must have a Bachelor's degree in a scientific discipline or foreign education equivalent & 5 years… more
- AbbVie (Chicago, IL)
- …. Job Description Purpose Responsible for leading and writing clinical and regulatory device and drug documents in support of company objectives for the ... support product approvals (eg briefing books, IND, protocol, CSR, NDA sections, and regulatory response as well as CER, IDE and PMA). Coordinates the review,… more
- Element Materials Technology (Fairfield, OH)
- …compliance with laboratory procedures, quality, and safety requirements + Scientific /Mathematical aptitude Education and/or Experience + High school diploma ... safe, compliant and fit for purpose. From early R&D, through complex regulatory approvals and into production, our global laboratory network of scientists,… more
- J&J Family of Companies (Titusville, NJ)
- …United States of America **Job Description:** **Senior Manager/Associate Director, Regulatory Medical Writing X-TA** At Johnson & Johnson Innovative Medicine, ... best talent for a **Senior Manager** **/Associate Director** , ** Regulatory Medical Writing** within our Integrated Data Analytics &...proactive or lead role in terms of content and scientific strategy. Working with a high level of independence… more
- J&J Family of Companies (Spring House, PA)
- …https://www.jnj.com/innovative-medicine We are searching for the best talent for a **Manager, Regulatory Medical Writing** to support one or more of our therapeutic ... areas in within the X-TA Regulatory Medical Writing unit, Integrated Data Analytics & Reporting...role on assigned projects with respect to content and scientific strategy, timing, scheduling, and tracking. May consult with… more
- Charles River Laboratories (Ashland, OH)
- …accomplished) include, but are not limited to, those listed:_ + Function as lead writer for standard study reports. + Attend study meetings as applicable to assure a ... all protocol and amendment requirements are met. + Ensure reports meet regulatory and client requirements. + Generate, format, and/or review report components/text… more
- AbbVie (Mettawa, IL)
- …and considered for future opportunities. About the role: The Principal Medical Writer is responsible for providing writing support and advanced scientific ... of information and review of assigned writing projects. Serves as the scientific writing expert for the department. Responsibilities + Serves as medical writing… more
- Dominion Energy (Richmond, VA)
- …staff to obtain appropriate environmental permits, develop and interpret scientific studies, maintain environmental compliance, and create corporate environmental ... regulatory positions across all business areas and environmental media...at. **Nearest Major Market:** Richmond **Job Segment:** Environmental Engineering, Project Manager, Six Sigma, Technical Writer , Engineer, Engineering, Management,… more
- Olympus Corporation of the Americas (Center Valley, PA)
- …. **Job Description** The Clinical Evaluation Manager/Senior Clinical Evaluation Report Writer reports directly to the Regional Lead, Clinical Evaluation Reporting, ... MSA. The individual creates CERs in support of EU-MDR regulatory approval strategies across Olympus business unit portfolio and meet timelines according to projects… more