Able to maintain the quality systems such as Lab Control, investigation management, materials management,document control and training to ensure control of the manufacturing process.Review GMP documents and correction findings.Understand and interpret written material as well as explain those materials and new regulations to team members and employees.Conduct audits,training programs,data and documentation reviews and analysis.

I worked Clinical Study Coordinator able to screen subjects for clinical trials, consent subjects, collect patients medical history, perform vital signs, EKG, drawn and process blood and other clinical procedures as per protocol.Data management,Open AE an SAE and Drugs Accountability.

Assist Patients with their daily activities of living.Assist with first Aid.Assist Patients with personal hygiene and skin care.Maintain clean in order to clients health and safety.