Areas of Experience

Qualified Research Consultant

Every clinical trial is a complex project that requires not just adequate planning but also a skilled partner to be successful. With industry-leading knowledge and over 35 years of experience as a clinical monitor and owner of a national IRB, you can trust me to provide you with the highest-quality consulting solutions and I work closely with the FDA.

Background

In 1985, I started my own consulting business, Florida Clinical Research, and have operated it for over 35 years. I then started and directed an Institutional Review Board in 1986, which offered its services nationally until 1999. Furthermore, I have extensive experience in teaching and lecturing to medical schools, universities, and professional associations nationally and internationally in the following areas:

Good Clinical Practice (GCP) Issues
FDA Regulations & Requirements
IRB & Regulatory Issues
Assists With Budget Planning
& Proposals