Open Research Office sessions bring together researchers and administrative personnel to address topics vital to launching, sustaining and completing a successful clinical or behavioral research project, including but not limited to:
- contracts and agreements
- budgets
- accounts receivable
- IRB submissions and regulatory compliance
- protocol development and regulatory guidance
- Central Study Registration, OnCore and Click support
- issues specific to your clinical or behavioral study
Bring your questions and specific concerns for on-the-spot, expert advice, guidance and instruction at any stage of your project. We're also seeking suggestions for future presentation topics.
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