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  1. High School Teachers/Writers to Create Learning Materials (TX)

    We're a new educational technology startup looking for help from current teachers, educators, or writers in helping us create and curate new learning materials for classrooms and individual learners. We're building a number of fun free educational tools that leverage recent advances in learning science (e.g., spaced repetition, recall testing) and technology-related advances (e.g., open source materials, adaptive algorithms for personalized learning). Our first product, Geknowm Pictorial, uses image ...

  2. High School Teachers/Writers to Create Learning Materials (Austin, TX)

    We're a new educational technology startup looking for help from current teachers, educators, or writers in helping us create and curate new learning materials for classrooms and individual learners. We're building a number of fun free educational tools that leverage recent advances in learning science (e.g., spaced repetition, recall testing) and technology-related advances (e.g., open source materials, adaptive algorithms for personalized learning). Our first product, Geknowm Pictorial, uses image ...

  3. Senior/Principal/Team Lead Medical Writer

     Senior/Associate Principal/Principal/Team Lead Medical Writers This leading regulatory writing company with US locations in CA (San Diego), TX (Austin), TN (Nashville), PA (Malvern), DE (Wilmington), and MA (Cambridge) is seeking regulatory writing talent at a variety of levels for on-site, full-time, permanent positions. The company enjoys a 25 year-plus track record of stability and offers its employees excellent growth potential, competitive salaries, profit sharing, and benefits, as well as, ...

  4. Regulatory Medical Writer (home based)

    We are in need of strong writers for a large CRO in the East Coast! Must have written all of the following: NDA submissions, Protocols, Narratives, Case Report Studies, and Inform Consent forms   Write clinical documents for submission to regulatory authorities, including but not limited to: briefing documents, clinical development plans, previous human experience summaries, human pharmacology summaries, investigator brochures, study protocols, model informed consents, interim and final ...