Executive / Sr. Executive (Academics)

• Serves as primary study coordinator for research protocols.
• Directs the conduct of clinical studies (according to Schedule Y) to ensure adherence to the research protocol and provides bimonthly updates to Principal Investigator on study progress.
• Screens patient records, databases, and physician referral summaries for identification of prospective candidates for research protocols.
• Participates in initiation visits/investigator’s meetings for assigned clinical trials (may involve travel) and implements these trials according to a deadline schedule mutually agreed upon by PI and sponsor.
• Develops study working folders for assigned protocols to outline guidelines for protocol compliance and to assure complete source documentation.
• Developing a preliminary budget and verify all costs
• Helping PI negotiate the study budget direct costs with sponsor to cover all costs (F&A costs are not negotiable)
• Educates human subjects for participation in investigations.
• Educates clinic/hospital personnel for participation in protocol conduct, data collection process, and related conceptual issues as applicable.
• Maintains consistent enrollment in protocols and provides monthly written documentation of screening/enrollment/follow-up activities.
• Coordinates the collection of data according to the research protocol, operations manual, and case report form guidelines within the budgetary guidelines.
• Instructs Principal Investigator on procedures and tests that need to be performed in compliance with the study protocol and advises Principal Investigator on the results of procedures and tests; calling to attention findings of clinical importance.
• Documents research related examinations, procedures, tests, and other activities in appropriate clinic or hospital charts.
• Data collection and maintaining patient database.
• Perform such duties as are allotted to you.

Any other professional and administrative duties delegated as and when required