Teams at Frontage Laboratories, Inc

Audits study data, reports, facilities, SOPs, and documentation for GLP compliance; tracks CAPAs and deviations; conducts internal audits and regulatory training; maintains vendor qualifications; and supports client and regulatory audits.

Manage clinical trial data transfers and internal reporting between Frontage, clients, and laboratory systems. Responsibilities include defining data elements, configuring LIS/LIMS data capture, creating data transfer agreements, building reporting and transfer templates, developing import/export processes, verifying data accuracy with Quality Assurance, and ensuring timely compliance with HIPAA, GDPR, GCP, GLP, CAP, and CLIA requirements.

Administer Provantis for nonclinical toxicology studies, including study setup, data acquisition, reporting, data tables, troubleshooting, documentation, training, validation, upgrades, and user support. Collaborate with Study Directors, IT, Quality Assurance, and toxicology teams to maintain GLP compliance, data integrity, inspection readiness, and efficient study workflows.