AEM Author TekWissen LLCAEM AuthorMalvern, PA$55Maintains broad awareness of changing technology, applications, trends, client needs, and legislative changes to proactively support creation and testing of marketing/communication content. Overview TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients world-wide.
Clinical Document Author - Remote YO AI LabsClinical Document Author - RemotePhiladelphia, PennsylvaniaRemote$50–$80 / hourWe are seeking an experienced Medical Writer / Clinical Document Author to develop, review, and evaluate clinical and regulatory documents while ensuring scientific accuracy, regulatory compliance, and high-quality medical writing. Verify scientific accuracy using source data, TFLs (Tables, Figures, and Listings), and study documentation.
2027 Future Talent Program - Computer Scientist - Agentic & Augmented Authoring Systems - Co-op Merck & Co Inc2027 Future Talent Program - Computer Scientist - Agentic & Augmented Authoring Systems - Co-opWest Point, PAThe ideal candidate will have experience with the principles of Natural Language Processing (NLP) in addition to agent-based concepts including orchestration frameworks (such as LangChain, CrewAI, LlamaIndex, or equivalent), tool calling, and API integration. NDS employees evaluate Lead Op candidates and preclinical toxicity of drug development candidates, providing a mechanistic understanding of drug-induced toxicity and assessing implications for human safety.
Medical Writer / Clinical Document - Remote YO AI LabsMedical Writer / Clinical Document - RemotePhiladelphia, PennsylvaniaRemote$50–$80 / hourWe are seeking an experienced Medical Writer / Clinical Document Author to develop, review, and evaluate clinical and regulatory documents while ensuring scientific accuracy, regulatory compliance, and high-quality medical writing. Verify scientific accuracy using source data, TFLs (Tables, Figures, and Listings), and study documentation.
Manager, External Affairs Rocket Pharmaceuticals IncManager, External AffairsCranbury, NJ$120,000–$160,000 / yearThis role will support the execution of external communications initiatives by developing high-quality written materials, coordinating cross-functional projects, supporting scientific communications, and ensuring consistent messaging across external stakeholders. We encourage applicants with at least four years of relevant experience who demonstrate strong biotechnology or life sciences expertise, exceptional writing capabilities, and a record of successfully managing cross-functional communications initiatives to apply.
Senior Technical Writer - Madcap Flare & AI Expert Wolters KluwerSenior Technical Writer - Madcap Flare & AI ExpertPhiladelphia, PARemote$60,700–$106,000 / yearThis is an exciting opportunity for a technical writer who enjoys learning complex software, partnering with Product Managers and Subject Matter Experts, and turning complicated functionality into clear, intuitive documentation for end users. We've been recognized by employees as a European Diversity Leader in the Financial Times, as one of Forbes America's Best Employers for Diversity in 2022, 2021 and 2020 and as one of Forbes America's Best Employers for Women in 2021, 2020, 2019 and 2018.
Senior Manager, Medical/Regulatory Writer Immunocore Holdings PlcSenior Manager, Medical/Regulatory WriterRadnor, PAVacancy NameSenior Manager, Medical/Regulatory Writer Vacancy NoVN831 Employment TypeFull Time Location of roleGaithersburg, MD, Radnor, PA, Remote, US DepartmentRegulatory Affairs Key ResponsibilitiesThe Senior Manager, Medical/Regulatory Writer will be accountable for leading and overseeing the medical and scientific regulatory writing for assigned programs to support submissions from first-in-human studies through product registration. Authoring or supervising the preparation of other regulatory documents required for Health Authority submissions, including but not limited to: Clinical Summaries (Clinical Overview, ISS/ISE, PK/PD summary, Advisory Committee Briefing document), Investigator Brochure(s), DSURs, other regulatory documents including briefing documents for health authorities, responses to Health Authority questions, etc.
Medical Writer - Remote YO AI LabsMedical Writer - RemotePhiladelphia, PennsylvaniaRemote$50–$80 / hourWe are seeking an experienced Medical Writer / Clinical Document Author to develop, review, and evaluate clinical and regulatory documents while ensuring scientific accuracy, regulatory compliance, and high-quality medical writing. Verify scientific accuracy using source data, TFLs (Tables, Figures, and Listings), and study documentation.