• Led a team of clinical research coordinators conducting clinical trial procedures as per protocol.• Provided training and performance evaluations to the study team.• Managed study documentation, including consent forms and case report forms.• Conducted site initiation visits (SIVs), Pre-Selection Visits (PSVs), and close-out visits.

 Prepared laboratory specimens for analysis, monitoring tests and procedures, and shipped frozen specimens. Collaborated with principal investigators and study sponsors, monitor and report serious adverse events. Organized and prioritized work to maximize effectiveness and productivity. Updated and maintained clinical systems within project timelines. Conducted recruitment and telephone screening of prospective study participants. Aided on clinical research studies per study guidelines and protocols.