- System One (Park Ridge, NJ)
- Title: Sr Regulatory Writer - R&D Location: Park Ridge, NJ area Schedule: M-F Full Time Type: Direct Hire Responsibilities: Our client is seeking Regulatory ... device, cosmetic, disinfectant (EPA, DIN) and general household products areas. The Senior Writer will lead and drive the technical (CMC) writing to accelerate the… more
- BeOne Medicines (Emeryville, CA)
- …Required: + At a minimum 4 years' relevant industry experience as a regulatory medical writer with a BA/BS degree; PhD/PharmD in life sciences ... **General Description:** The Senior Medical Writer is responsible for writing, editing, and formatting... is responsible for writing, editing, and formatting clinical regulatory documents that conform to domestic and/or international … more
- Edwards Lifesciences (Naperville, IL)
- …defining features for the development team to creating engaging release notes and regulatory materials, the Technical Writer ensures that all written content ... part of our inspiring journey. **How you will make an impact:** The Technical Writer will play a crucial role in supporting the development and release of… 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 - a .… more
- Holtec International (Covert, MI)
- …and historic undertaking for the industry and the nation! JOB SUMMARY The Exam Writer develops and administers Regulatory Exams in accordance with NUREG 1021, ... Exam Writer Holtec Decommissioning International (HDI) is currently seeking...for assigned programs, including interfacing with INPO and Nuclear Regulatory Commission (NRC) as required. + Interacting professionally with… more
- University of Miami (Miami, FL)
- …Development Office (PDO) has an exciting opportunity for a Full Time Scientific Writer (Medical Writer ) to work Remotely. CORE JOB SUMMARY The Scientific ... Writer analyzes scientific data and translates complex scientific concepts,...of clinical trials including protocol and ICF development, institutional regulatory submissions (Protocol Review and Monitoring Committee [PRMC] and… more
- Kelly Services (Bloomington, IN)
- Technical Writer (Bloomington, IN) Our client in the medical devices/ life sciences/pharma space, is currently in need of a Technical Writer for a large project ... or capped end date, however, this project is expected to take 3-6 months. Technical Writer will need to sit onsite in at the client's facility in Bloomington, IN, as… more
- Terumo Neuro (Aliso Viejo, CA)
- …years of scientific experience. 3. Demonstrated experience in the development of regulatory / clinical submissions (preferably as a medical writer for ... **12640BR** **Title:** Sr. Medical Writer **Job Description:** **INNOVATION STARTS WITH YOU** Are...job duties include: + Collaborating with the clinical & regulatory teams to write clinical documents for regulatory… more
- Houston Methodist (Houston, TX)
- The Scientific Writer at Houston Methodist, Department of Digital Health Innovation and Implementation Research position must have experience writing and editing a ... on impact ranging from clinical to operational and financial. Writer should be comfortable going in 'cold' to 'find...sponsors as to how best to present data considering regulatory agency requirements. + Prepares moderately complex documents and… more
- State of Colorado (Denver, CO)
- …Protection Intern - Water Quality Permit Writer - 2461 Print (https://www.governmentjobs.com/careers/colorado/jobs/newprint/4873290) Apply Environmental ... Protection Intern - Water Quality Permit Writer - 2461 Salary $4,872.00 - $5,845.00 Monthly Location...groundwater. Additional core work assigned to the unit includes regulatory development and issuance of reuse notices of authorization… more
- ICON Clinical Research (New York, NY)
- Medical Writer II- Farmingdale, NY- Hybrid ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive ... join us on our mission to shape the future of clinical development. **Medical Writer II- Farmingdale, NY- hybrid work pattern** We are currently seeking a Medical … more
- Actalent (San Francisco, CA)
- Job Title: Principal Medical Writer IIJob Description The Associate Director, Principal Medical Writer II is responsible for developing clinical documents for ... submissions to regulatory authorities globally. You will provide strategic direction to...activities of multiple compounds and serve as the lead writer for individual summary documents. You will have a… more
- Abbott (Princeton, NJ)
- …medicines. Our 114,000 colleagues serve people in more than 160 countries. **Technical Writer ** **Working at Abbott** At Abbott, you can do work that matters, grow, ... Our **Princeton, NJ** location has an opportunity for a **Technical Writer ** in the Instrument Operations Software technical group within **Abbott Point… more
- System One (New Haven, CT)
- Job Title: Medical Writer (part time) Location: Northeast (EST) candidates preferred Hours: 30 hours/month (7-8 hours/week) Type: Contract (C2C or W2) Job Purpose ... The Translational Research Medical Writer plays a key role in the development and...(Module 2). The role ensures document quality, consistency, and regulatory compliance while collaborating closely with internal and external… more
- Stony Brook University (East Setauket, NY)
- Digital Content Writer **Position Summary** As a Digital Content Writer , you will play a crucial role in crafting engaging and informative content that connects ... service line landing pages and campaigns. The Digital Content Writer reports to the Director Digital Marketing for Stony...complete a 4 panel drug screen * + Meet Regulatory Requirements for pre-employment screenings. + Provide a copy… more
- Olympus Corporation of the Americas (Westborough, MA)
- …career ladder is between Sr. Engineer and Principal Eng. The Staff Technical Writer is responsible for all aspects of documenting all related documentation and ... Core Team Member. In this role, the Staff Technical Writer will execute all aspects of documenting all labelling...documentation updates to comply with EUMDR, FDA and other regulatory body requirements by incorporating customer inputs and ensuring… more
- AbbVie (San Francisco, CA)
- …LinkedIn. Allergan Aesthetics | An AbbVie Company Job Description Purpose The medical writer is responsible for providing clinical regulatory document support to ... and effective implementation of the clinical writing process. The medical writer : provides medical writing expertise for multiple compounds and/or projects within… more
- Leidos (Fort Belvoir, VA)
- **Description** Leidos is seeking a **Senior Technical Writer in Fort Belvoir, VA** to support large-scale migration and operations on a large, high-profile DOD ... mission partners operating in CONUS and OCONUS locations. The Senior Technical Writer will be responsible for writing, editing, proofreading and/or providing writing… more
- Million Air (Houston, TX)
- …Houston | Full Time Job Title: Aviation Sales Representative / Service Writer Department: Maintenance / Customer Service Reports To: Director of Maintenance ... highly motivated and knowledgeable Aviation Sales Representative / Service Writer to serve as the key point of contact...completed work orders are accurate, detailed, and compliant with regulatory requirements. + Scheduling & Planning: + Assist in… more
- NANA Regional Corporation (Oak Ridge, TN)
- …to satisfy clearance requirements from the Department of Energy. The Procedure Writer will support the ISED Document and Records Management Group Lead in ... provide specific instructions for task performance using PPA and ORNL writer 's guides. + Performs independent verifications and conducts independent validations of… more
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