⏩ Coordinate and managing clinical trials in compliance with applicable regulations and standard operating procedures (SOPs) ⏩ Ensure the timely completion of study tasks and met project timeline ◾️Patient Requirement ◾️Screening Procedure ◾️Content Participants ◾️Randomizing the subjects ◾️Scheduling the Visits ◾️subject follow-up procedure⏩ Conduct and document study visits and… Show more ⏩ Coordinate and managing clinical trials in compliance with applicable regulations and standard operating procedures (SOPs) ⏩ Ensure the timely completion of study tasks and met project timeline ◾️Patient Requirement ◾️Screening Procedure ◾️Content Participants ◾️Randomizing the subjects ◾️Scheduling the Visits ◾️subject follow-up procedure⏩ Conduct and document study visits and procedures, including vital signs, medical history, and medication review⏩ Collaborate with Investigator, Sponsor and other team members ⏩ Maintenance of study protocols, drug accountability and ensuring compliance with regulatory documents⏩ Collecting the clinical trial data, and managing the study data, maintaining the accurate data and organized records⏩ Prepare and maintain regulatory documents and EC submissions, such as IRB application, progress reports, and safety reports⏩ Assured timely reporting of Adverse Events(AEs) & Serious Adverse Events (SAEs) Show less