Teams at Fortrea

The Principal Biostatistician will lead complex clinical trials, develop and review statistical analysis plans, and provide programming support. Responsibilities include project management, mentoring junior staff, and presenting findings at meetings.

The Associate Director will manage pharmacovigilance operations, oversee staff, ensure compliance with safety services, and support business development activities.

Own clinical delivery and operational oversight of trials from site identification through database lock. Manage start-up, regulatory/ethics submissions, budgets, KPIs, vendor performance, monitoring strategy, TMF quality, site payments, recruitment strategies, and cross-functional client communications to ensure compliance, data integrity, patient safety, and inspection-readiness.