- Tris Pharma (Monmouth Junction, NJ)
- …an opening in our Monmouth Junction, NJ facility for an experienced SR. Medical Writer . This is an individual contributor role. SR. Medical Writer provides ... writing expertise and leadership in the preparation of clinical and regulatory documents. Collaborating closely with cross-functional teams to ensure accuracy and… more
- Aequor (Swiftwater, MN)
- …documents (SOP's, guidelines, validation master plans, etc.) to ensure compliance with regulatory requirements. Must be able to work quickly with a high degree ... of accuracy. Must possess sound interpersonal and information gathering skills, be able to relate well to others at all levels throughout the organization and have the ability to work in a team environment, effectively interacting with others. Review current… more
- Formation Bio (New York, NY)
- … regulatory documents to support drug development programs. Experience as lead writer for key clinical and regulatory documents required. Experience mentoring ... operational plans to support Formation Bio Clinical Development activities. The Medical Writer will have responsibilities to write or facilitate the writing of key… more
- 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
- United Rentals (Bladensburg, MD)
- …will play a key role in customer satisfaction, operational efficiency, and regulatory compliance. **Key Responsibilities:** **Service Writer Duties:** Manage Due ... rental provider, **come build your future with United Rentals!** **SERVICE WRITER /TITLE CLERK:** This dual-role position is responsible for managing rental service… 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
- 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
- Eurofins (Lancaster, PA)
- …origin, traceability and purity of biological substances and products. Technical Writer : Manage the production of simple scientific and technical documents ... technical documents, training material and other written material. Senior Technical Writer : Manage the production of complex scientific and technical documents… 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
- Craig Technologies (Oak Ridge, TN)
- Title: UPF Startup Technical Writer (Uranium Processing Facility) Location: Oak Ridge, TN Clearance: Must be able to obtain and maintain a DoD Secret Security ... clearance, as applicable. Job Summary: The primary role of the UPF Startup Technical Writer will be to support the Startup team with Test Packages to ensure… 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
- Astrix Technology (Chicago, IL)
- **Medical Writer ** Medical Writer Chicago, IL, US Pay Rate Low: 85,000 | Pay Rate High: 125,000 + Added - 02/06/2025 Apply for Job At Astrix, we're expanding our ... pharmaceutical companies, all seeking professionals who can craft high-quality regulatory and clinical documents that support global submissions and advance… 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
- Amazon (Kirkland, WA)
- …without reliable connectivity. We are seeking a detail-oriented and highly skilled Technical Writer to join the Kuiper team. The ideal candidate will be responsible ... and maintaining technical documentation that supports engineering, manufacturing, and regulatory compliance. This includes manuals, specifications, user guides, maintenance… more
- Nanobiosym, Inc. (Cambridge, MA)
- Cambridge, MA, USA | Contract Job Title: Scientific Writer (Onsite Consultant)Location: Cambridge, MA About the Role: We are seeking an experienced Scientific ... Writer with a strong background in scientific editing and...objectives. + Translate technical research into accessible content for regulatory submissions, funding bodies, and public communication. + Review… more
