Fortrea
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Biotech
The Associate Director will manage pharmacovigilance operations, oversee staff, ensure compliance with safety services, and support business development activities.
Biotech
Lead and deliver global oncology clinical projects by managing scope, schedule, budget, quality, risks, and stakeholder communications. Oversee cross-functional teams, ensure regulatory and GCP compliance, mentor staff, support business development, and maintain project KPIs and resource planning.
Biotech
Lead clinical data management from study start-up to database lock, oversee DM deliverables and teams, liaise with sponsors, manage timelines/budgets/scope, mentor staff, ensure GCP/SOP compliance, coordinate cross-functional biometrics activities, support audits, and drive process improvements and client satisfaction.
