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Administrative
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Liaison with sponsors, study correspondence and communications
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Preparation and submission of COMIRB application packet, tracking and ongoing interactions with COMIRB
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Ongoing regulatory reporting back to sponsor, and COMIRB
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Development and submission of Informed Consent Forms and HIPPA forms
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Budget preparation and contract negotiations, sponsor billing and tracking of payments. Reconciliation of budgets with allocated FTEs
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Web-based clinical trials registry (Service not immediately available)
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Study site (UCH, VA, DHHA) research review submission
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