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Experience developing optimized modules in C#/C++ within Unity and/or Unreal Engine Experience with database management systems Where to apply Website https://www.timeshighereducation.com/unijobs/listing
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, protocol submissions, and SOPs. May train others in these policies and processes. Is responsible for all aspects of managing and documenting Investigational Product (IP); including arrival, storage, tracking
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. Operations: Recognizes when typical agreements (MTAs, CDAs, DUAs, DTAs, etc.) are necessary and alerts appropriate parties. Prepares FDA regulatory submissions in collaboration with ORAQ, including development
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Assistance Program (EAP) Annual Leave Sick Leave 13 Paid Holidays (including an extended December holiday) Paid Parental Leave Professional Development Opportunities Quicklink for Posting https
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tools and a catalogue of the capabilities of IDIVAL's research groups, offering them strategic support. Prepare reports on results, impact monitoring and sustainability analysis of European actions
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directly with departmental patent coordinator and internal legal counsel (OGC) on patent costs and filing tactics with outside patent law firms. Develops marketing materials and website information on IP
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-to-day regulatory and safety operations for multiple, complex oncology clinical trials and research studies, including those involving Investigational Products (IP). Your work will ensure compliance
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, medium and long-term strategic development, and signpost best practice to produce, protect and track our IP and knowledge. Possessing a degree or relevant experience in a medical or healthcare subject and
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support for BAS logic and graphical interfaces, ensuring proper functionality and system performance. Troubleshoot BAS networks, including IP-based controllers, BACnet, Modbus, and LonWorks. Review
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Harvard’s Office of Technology Development (OTD) and Office of Sponsored Programs (OSP). Anticipates and flags agreement concerns such as data sharing, IP, and publication rights. Post-award works with HBS