Sub-Investigators

At our clinical trial sites, we are committed to advancing medical science through rigorous and ethical research practices. Central to this mission is our team of Sub-Investigators (Sub-Is), who collaborate closely with Principal Investigators (PIs) to ensure the successful execution of our studies.​ Sub-Investigators are essential members of our clinical research team, responsible for performing critical trial-related procedures and making important study-related decisions under the supervision of the PI. Their duties include:​ Participant Recruitment and Screening: Identifying and evaluating potential study participants to ensure they meet eligibility criteria.​ Informed Consent Process: Ensuring participants are fully informed about the study's purpose, procedures, potential risks, and benefits before obtaining their consent.​ Clinical Assessments: Conducting medical examinations, administering investigational treatments, and closely monitoring participants' health throughout the trial.​ Data Management: Collecting, recording, and maintaining accurate study data in compliance with regulatory standards.​ Safety Monitoring: Observing and reporting adverse events or side effects to the PI and relevant authorities, prioritizing participant safety.​ Regulatory Compliance: Ensuring all trial activities adhere to Good Clinical Practice (GCP) guidelines and other applicable regulations.​ Our Sub-Investigators are highly qualified professionals with extensive experience in clinical research. They are dedicated to upholding the highest standards of participant care and data integrity, contributing significantly to the success of our clinical trials.