Medical Monitor - Safety Analyst I Clinical Trial/CRO

The Medical Monitor/ Safety Data Analyst processes Adverse Event (AE) and Serious Adverse Event (SAE) cases promptly and with medical accuracy. The Medical Monitor/ Safety Data Analyst will also assist the Head of Safety and Pharmacovigilance Department with Medical Coding and Medical Monitoring activities and oversees the overall conduct of pre- and post-marketing studies regarding safety of the subjects for his/her studies, and as a back-up for other Medical Monitors.