- Actalent (Parsippany, NJ)
- Job Title: Technical Writer - Compliance Location: Parsippany, NJ Employment Type: 12-Month Contract Industry: Pharmaceuticals / Biotechnology About the Role We are ... seeking a detail-oriented and experienced Technical Writer - Compliance to join our Quality or Manufacturing team. In this role, you will be responsible for… more
- California State University (Northridge, CA)
- College and Marketing Communications Writer Job no: 549159 Work type: Staff Location: Northridge Categories: Unit 9 - CSUEU - Technical Support Services, ... Duties Under general supervision, the College and Marketing Communications Writer creates foundational and compelling cases for programs, collaborates… more
- Actalent (Santa Clara, CA)
- …releasing design change orders. Provide oversight on proper documentation for regulatory submissions. Essential Skills Medical device experience and ... Job Title: Technical Writer Job Description Collaborate with various teams to...clear documentation for internal and external use in a medical device environment. Responsibilities Distill technical information into accessible… more
- Integrated Resources, Inc. (Princeton, NJ)
- Job Description: The primary responsibilities of an Associate Director Medical Writer include, but are not limited to, leading key medical writing projects ... and summaries and overviews of nonclinical and clinical information). The Associate Director Medical Writer has a broad range of experience in pharmaceutical … more
- Allen Spolden (New Brunswick, NJ)
- Job Description The Medical Writer will primarily work on the development and delivery of high-quality documents such as Clinical protocols, protocol amendments, ... meet business objectives. Ability to initiate and generate with limited supervision medical , regulatory , and clinical documents within a reasonable timeframe… more
- Vantive (Deerfield, IL)
- …possibilities. Your Role Responsible for the written communications between Vantive and regulatory agencies in response to questions or requests within the Vantive ... system. Responsible for following and (as needed) adjusting the regulatory agency communications process, globally and company-wide. Responsible for tracking… more
- Ogilvy Health US (Parsippany, NJ)
- …all program materials to appropriate team members (including but not limited to Medical Writer , Medical Director, Program Director, Account Director Art, ... routing, track and manage incorporation of client and MLR ( Medical , Legal, Regulatory ) Review comments and approvals As applicable, participate in client… more
- Oaktree Capital Management, LP (Dallas, TX)
- …Questionnaires (DDQs) for Oaktree clients and prospects globally. As a Proposals Writer /Due Diligence Project Manager, you will play an important role in the ... auxiliary documentation such as board lists, client representative lists and regulatory and compliance information; Participating in quality assurance reviews for… more
- SWCA Environmental Consultants (Salt Lake City, UT)
- …for improvement. Permitting: Prepare and submit stormwater permit applications to regulatory agencies. Coordinate with regulatory agencies to obtain necessary ... and other related documents. Communicate complex technical information to clients, regulatory agencies, and other stakeholders in a clear and understandable manner.… more
- AECOM (Chelmsford, MA)
- …and regulations. Strong communication skills in coordinating with clients, sub-consultants, regulatory agencies, and members of the public to accomplish assigned ... and methods. Self-starter and ability to take initiative. Experienced technical writer . Additional Information This position does not offer relocation assistance.… more
- ThermoFisher Scientific (Greenville, NC)
- …(FSP) Team and are seeking candidates based in the US! As a remote-based Senior Medical Writer within the FSP team, you will provide high-quality medical ... will possess the versatility to author both clinical and preclinical regulatory documents, with therapeutic area expertise in infectious diseases and/or oncology.… more
- BeOne Medicines (Emeryville, CA)
- …Education/Experience Required: + At a minimum 4 years' relevant industry experience as a regulatory medical writer with a BA/BS degree; PhD/PharmD in life ... **General Description:** The Senior Medical Writer is responsible for writing,...+ Ensure clinical documents adhere to BeOne standards and regulatory guidelines. + Coordinate and manage contract medical… more
- Ascendis Pharma (Princeton, NJ)
- …mission of developing new and potentially best-in-class therapies to address unmet medical needs. Our culture fosters a place where skilled, adaptable, and highly ... - and have experience within the pharma industry, and 8+ years within Medical Writing. Furthermore, you have: + Experience in authoring clinical/ regulatory … more
- Abbott (Maple Grove, MN)
- …for a Medical Writer / Clinical Evaluation Reporting (CER). The Medical Writer on our Regulatory Clinical Evaluation team provides technical and ... experience. + 3 years' progressively more responsible experience as a technical writer in a medical or high technology (preferably biotechnology) environment.… more
- State of Colorado (Denver, CO)
- …Protection Intern - Water Quality Permit Writer Print (https://www.governmentjobs.com/careers/colorado/jobs/newprint/5009925) Apply Environmental Protection Intern ... - Water Quality Permit Writer Salary $2,293.85 - $3,387.69 Biweekly Location Denver, CO Job Type Full Time Job Number FAA02443-07/16/25 Department Department of… 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 ... template creation or refinement. + Stay up to date with clinical and regulatory developments relevant to medical writing. **Qualifications:** + Bachelor's degree… more
- Nuclear Fuel Services (Erwin, TN)
- …the safe operation of equipment, procedure flow and usability, and adherence to regulatory requirements and writer 's guidelines. + Interface with Subject Matter ... of Energy and NASA facilities. BWXT's technology is driving advances in medical radioisotope production in North America and microreactors for various defense and… more
- System One (Cleveland, OH)
- Job Title: Director / Senior Director Medical Writer Location: CST or EST candidates willing to work EST Type: Direct Hire Compensation: $165000 - $250000 ... Work Model: Remote As a Director or Senior Director, Medical Writer you will be responsible for... documents, reports and protocols through implementation of the regulatory medical writing process in collaboration with… more
- Actalent (Philadelphia, PA)
- Lead Medical Writer Job Description We are seeking a highly experienced Senior Medical Writer to join our team and contribute significantly to our ... 10+ years of medical writing experience. + Experience with clinical and regulatory documents. + Experience working with a sponsor, preferably in small pharma. +… more
- Regeneron Pharmaceuticals (Armonk, NY)
- The Senior Medical Writer (SMW) works with team members and independently to write the content of clinical documents that may include CSRs, protocols, ICFs, ... variety of therapeutic areas. Opportunities to contribute to other regulatory documents may be provided. The SMW tracks their...help ensure appropriate content for inclusion. **As a Senior Medical Writer , a typical day may include… more
