I have served as a Principal Investigator in clinical trials and clinical research for 10 years. My extensive research experience covers a wide range of therapeutic areas including asthma, allergy, immunology, pediatrics, cardiology, endocrinology, opthalmology, analgesia/pain, women’s health, psychology, vaccine studies, and healthy volunteers. I strive to bridge pharmaceutical research with compassionate and practical global applications.
My comprehensive understanding public health and population studies, as well as my experience with a wide range of clinical trials, allows me to be instrumental in several aspects of clinical trial success from population analysis to clinical trial implementation. I am well versed in Good Clinical Practice (GCP) guidelines and FDA regulations.
I can provide consulting services to both clinical research sites and Sponsor organizations on:
- Protocol development and design
- Clinical trial implementation
- Investigator training
- Standard Operating Procedures (SOP) development
- Audit preparation
- Process development and improvement
- Medical monitoring