Teams at The Geneva Foundation

Coordinates regulatory compliance for human-subjects research studies, including IRB and IACUC submissions, amendments, reports, study records, participant tracking, site monitoring, and investigator support. Maintains regulatory documentation, ensures FDA and ICH guideline compliance, manages award deliverables, develops internal controls, coordinates research meetings, and supports participant safety, confidentiality, and collaboration among investigators, research staff, sponsors, and funding organizations.

Lead and manage pre-clinical research projects at a DoD university biotech center focused on hematopoiesis and on-demand blood products. Oversee experimental design and execution, supervise staff, ensure regulatory compliance (GLP, IACUC/IRB), prepare reports and SOPs, analyze research portfolios, support proposal development and grant success, and coordinate multidisciplinary teams with government and contract researchers.

Coordinate and administer clinical research studies including recruitment, data collection, regulatory documentation (IRB/IACUC), protocol implementation, staff oversight, and communication with investigators and sponsors. Ensure participant safety, compliance with GCP/ICH/CFR, and maintain study records and reports.