Job Description

• Accountable for all aspects and progress of clinical trial from study planning activities to study execution. • Verify that the researcher has adequate qualifications and resources, as well as facilities, including laboratories, equipment and staff are adequate for safety and properly conduct of the clinical study throughout the study period. • Identify and resolve the issues (logistical, methodological, and technical) proactively occurring during a study and recommend solutions. • Proper collection and archiving the essential study documentation. • Timely and accurately execution of monitoring plan. • Prepare reports based on demand; prepare adverse event report and progression report. • Ensures realization of expenses and planned budget are balanced and tracks accordingly.