Perform all activities related to management of grant accounts. This includes setup, award management, invoicing/reporting and award closure

Perform all activities related to management of grant accounts. This includes setup, award management, invoicing/reporting and award closure

Perform all activities related to management of grant accounts. This includes setup, award management, invoicing/reporting and award closure

Perform all activities related to management of grant accounts. This includes setup, award management, invoicing/reporting and award closure

I work to process subaward agreements by reviewing and negotiating the agreements to ensure that all institutional requirements are met.

Perform Medicare Coverage Analysis including review of studies submitted for evaluation for Medicare Coverage Analysis determination, budget preparation, invoicing and check processing.

Prepare and submit all regulatory documents as each new study comes in for submission. This includes processing the 1572, financial disclosure forms, drafting the informed consent for IRB submission, completing the IRB submission and addressing all concerns with the IRB until approval, processing the study through the Clinical Trial Management System. Track and submit all new submissions, amendments, continuing renewals, safety reports, etc. through the eIRB program. Make sure regulatory binders are kept up-to-date by preparing the regulatory binders for the clinical studies coordinator once the study has been approved. Conduct pre-monitoring visits to review regulatory binders and check for accuracy of research data. Make sure that all files are kept up-to-date. This includes making sure that all approvals and approved documents are included in the files and making sure the files are complete once the clinical trial is ready for closeout. Maintain the files for CVs and medical licenses for all the Clinical Studies Principal Investigators, Sub-Investigators and study staff.

Prepare and submit all regulatory documents as each new study comes in for submission. This includes processing the 1572, financial disclosure forms, drafting the informed consent for IRB submission, completing the IRB submission and addressing all concerns with the IRB until approval, processing the study through the Clinical Trial Management System. Track and submit all new submissions, amendments, continuing renewals, safety reports, etc. through the eIRB program. Make sure regulatory binders are kept up-to-date by preparing the regulatory binders for the clinical studies coordinator once the study has been approved. Conduct pre-monitoring visits to review regulatory binders and check for accuracy of research data. Make sure that all files are kept up-to-date. This includes making sure that all approvals and approved documents are included in the files and making sure the files are complete once the clinical trial is ready for closeout. Maintain the files for CVs and medical licenses for all the Clinical Studies Principal Investigators, Sub-Investigators and study staff.