SFCRI RESPONSIBILITIES

Collaborate with the Principal Investigator to conduct patient visits Market Investigators to sponsors and clinical research organizations
Negotiate contract language and budgets
Prepare all clinical trial advertisements
Assist in actively recruiting patients
Attend Investigator meetings
Complete feasibility questionnaires
Analyze protocols to determine the feasibility of the trial
Prepare and maintain all regulatory documents required for the review committees and the FDA according to ICH and GCP guidelines
Track patient visits and procedures
Pay outsourced procedures and patient stipends
Prepare for monitoring visits as dictated by the sponsor
(i.e. ensuring that administrative documents, patient charts, and case report forms are in good order)