SUMMARY Clinical Research Professional with more than 20 years experience in Phase II-IV clinical site management, regulatory compliance and monitor training for major pharmaceutical companies. Demonstrated expertise in electronic systems including CTMS, EDC, IVRS, CRF design, query management and corporate communications. Proven success in all aspects of clinical trials from study start up through close out in phase IIb-IV clinical research trials in a broad variety of therapeutic areas for international pharmaceutical companies.

Highlights:

• Protocol
• Clinical Research
• Research
• Audit
• Training
• Clinical Research Associate