Teams at Fortrea

Supports preparation, review, and coordination of pharmacovigilance aggregate reports, including PBRERs, PSURs, and PADERs. Performs database searches, data analysis, quality control, timeline monitoring, and stakeholder coordination. The role also mentors junior staff, supports project management, contributes to process improvements and CAPA activities, and participates in audits, inspections, training, and regulatory initiatives.

Coordinate site start-up activities and regulatory compliance for clinical studies, serving as primary site contact. Support site selection, submissions, document collection and TMF maintenance, contract/budget negotiation, CRF review, vendor coordination, and stakeholder communication to ensure timely site activation and audit readiness.

Serve as the FSP subject-matter expert and strategic partner to sales and BD, develop and grow FSP business with biotech and pharma clients, support RFI/RFP responses and pricing, manage pipelines in SFDC, lead client presentations, mentor account teams, and create long-term account plans to achieve sales targets and customer retention.