Summary of Qualifications: * More than 15-years experience in the healthcare field * Over five (5) years experience working in Clinical Research * Sound knowledge of Good Clinical Practices (ICH-GCP's) and FDA regulations * Advanced medical/scientific knowledge and medical terminologies * Use of electronic data capture systems (EDC) * Clinical Trial Management Systems (CTMS) and IVRS systems * Conversant with the design and review of Case Report Form (CRF) * Site Monitoring (including PSVs, SIVs, IMVs and COVs) to meet study expectations * Source data/document verification (SDV) * Adverse events (AE/SAE) reporting according to regulations and company policy * Reviewing protocol compliance, focusing on inclusion/exclusion requirements * Excellent oral and written communication skills * Ready and willing to accommodate frequent local, domestic or international business travels.

Highlights:

• Health Awareness
• Research
• Training
• Public Health
• Quality Assurance
• Test
• Management
• HIV
• Compliance
• Medical