Teams at Evolution Research Group

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.

Conducts independent monitoring of clinical trial sites, including qualification, initiation, interim, and close-out visits. Ensures compliance with protocols, SOPs, FDA regulations, ICH-GCP, and study timelines. Manages investigator site files, Trial Master File documentation, investigational product accountability, data queries, correspondence, action items, and monitoring reports. Requires extensive domestic travel, strong clinical research expertise, and at least five years of CRA experience.

Manages clinical research projects from start-up through completion, overseeing scope, budgets, timelines, study materials, vendors, sites, regulatory compliance, data review, reporting, and client communications. Leads multidisciplinary internal and external teams, develops protocols and clinical documents, reviews monitoring reports, supports inspections, and ensures deliverables meet contractual, protocol, SOP, and quality requirements. The role is fully remote with occasional off-site meetings and conferences.