Major Duties:
- Overseeing the R&D subcommittees.
- Pre-screens all protocols/projects prior to the official review.
- Acts as the SME and primary source to the official for guidance prior to formal approval.
- Works with the Bio-safety Committee, Clinical Research Workgroup (CRW), the Human Research Protection Program (HRPP) and IACUC to develop procedures to meet regulations.
- Reviews all projects to determine the required approvals and provides on-site assistance to the investigators and their staff.
- Act as scientific, technical advisor and authority to Director of Research Operations(DRO) and Associate Chief of Staff (ACOS) for Research and Development (R&D).
- Ensures that personnel meet the training and scope requirements for safety, animal, and human approval aspects of a specific project.
- Responsible for reviewing, analyzing, and interpreting expenditure report data of all approved funded grants are reported through R&D Information System (RDIS) and the national e-PROMISE database..
- Performs comparative analysis of Investigator expenditure history reports.
Specialized experience includes providing direct and indirect scientific and administrative support, in a hospital or academic Research environment, initiates actions to implement new policies and procedures based on granting and regulatory agency regulations, performs comparative analysis of expenditure history reports, pre-screens all protocols/projects prior to the official review, identifies disparities and communicates directly with the project owners, to validate and report all direct expenditures, and responsible for reviewing, analyzing and interpreting expenditure report data.
https://www.usajobs.gov/GetJob/ViewDetails/612664300
If you have any questions please contact [email protected] or call/text 415-759-1553.