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Found 2 jobs
    • Switzerland
    • Negotiable
    • Posted 18 days ago

    Responsibilities Prepare and/or co-ordinate the preparation of regulatory documentation to support Clinical Trial Applications/amendments in Europe (EU, UK (post-Brexit) and Switzerland). Support for rest-of-the-world clinical trial applications may be required Contribute to the regulatory strate...

    • San Francisco
    • Negotiable
    • Posted 18 days ago

    Location: (100% Remote Role) Pay Rate: Open Contract: 6 Months w/ Possible Extension Job Description The Technical Writer is responsible for converting scientific data into clear, scientifically sound, well-structured scientific, technical and regulatory documents intended for global health autho...