Dedicated CRA with 3 years' experience in clinical trials with broad background in clinical management of phase II and III clinical drug studies. Significant expertise in various indications implementation of study protocols and electronic data capture implementation of study protocols monitoring of study sites and on-site data management and collection of study-related documents. Excellent communication skills (both written and oral) and the ability to build effective relationships with trial center staff and colleagues.

Highlights:

• Cardiovascular
• Clinical Management
• Clinical Operations
• Clinical Research
• Collection
• Compliance
• Cyclic Redundancy Code (CRC)
• Data Entry