Unpaid Clinical Research Team Member/Intern

Looking for an opportunity to experience Clinical Research at the site level. The responsibilities will include, but not limited to:

-Identifying research opportunities and contacting potential sponsors

-Completing regulatory documents

-Facilitating peer review, administrative review, and approval

-Applying for Institutional Review Board (IRB) review

-Interacting with the sponsor, Research Team, pharmacy, IRB, finance, and other departments impacted by the research

-Developing study processes

-Developing study documents

-Educating staff and participants

-Pre-screening, screening, and enrolling subjects

-Implementing and adhering to the protocol

-Accounting for study funds

-Reporting adverse events

-Providing continuing and final IRB reports

-Assisting PI and Sub-I in execution of protocol

-Always Protecting study participants

-Ensuring the integrity of the data collected