Teams at Evolution Research Group

Coordinates Phase I–IV clinical trials under Principal Investigator and Site Director oversight. Responsibilities include reviewing protocols, preparing source documents, screening and enrolling participants, obtaining informed consent, scheduling visits, maintaining study records, entering data, tracking adverse events, ensuring GCP and protocol compliance, communicating with sponsors and regulatory organizations, and completing study closeout procedures.

Enters, updates, verifies, and maintains high volumes of sensitive healthcare data. Prepares reports and correspondence, protects confidential information, handles frequent phone communication, resolves data discrepancies, and collaborates with clinical and administrative teams to support accurate records and efficient workflows.

Conducts independent site monitoring for clinical trials, including qualification, initiation, interim, and close-out visits. Ensures compliance with protocols, SOPs, FDA regulations, ICH guidelines, and GCP. Manages investigator site files, trial master file documentation, investigational product accountability, data queries, site communications, training, and monitoring reports. Requires extensive travel and may mentor junior CRAs while working independently as a contractor.