Teams at Elite Clinical Network

Conduct Phase I–IV clinical trials as a Principal or Sub-Investigator while providing dermatologic care to adult participants. Responsibilities include screening and enrolling patients, assessing eligibility, overseeing safety and adverse events, documenting clinical and regulatory data, ensuring ICH-GCP and FDA compliance, collaborating with sponsors and research staff, participating in monitoring visits and audits, counseling patients, and supporting recruitment and retention.

Coordinates clinical trials and research studies, including participant recruitment, screening, informed consent, visit scheduling, specimen collection, basic clinical procedures, data entry, regulatory documentation, and communication with sponsors, monitors, and IRBs. Ensures protocol adherence, ethical conduct, accurate records, specimen accountability, and compliance with clinical research requirements.

Coordinates clinical trials and research studies, including participant recruitment, informed consent, visit scheduling, specimen collection and processing, clinical procedures, data entry, regulatory documentation, investigational product accountability, and communication with sponsors, monitors, and IRBs. Ensures protocols, ethical standards, GCP requirements, and visit windows are followed while maintaining accurate study records.