Information already provided in latest version of my CV.
Predominantly, managing the components of IRB, Informed Consents, high level review of financials with management, deliverables report, follow up procurement requirements; vendor management; understanding GCP and FDA requirements. Understanding the Code of Federal Regulations (CFR) and Federal Acquisition Regulations (FAR); sub-contract and contract management, consulting agreements; working to collate reports from study managers; leading calls and taking notes; proactive dissemination of information; collating highly complex technical presentations for meetings with scientists, federal agencies, foundations and pharmaceutical contacts; facilitating collaboration agreements with scientists not based in the United States.
Great benefits and flexibility
No career progression or adequate resource management