Teams at Fortrea

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

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.

Lead clinical data management from start-up to database lock for oncology studies, manage sponsor relationships, timelines, budgets, and junior DM staff; coordinate with biometrics, EDC, SAS, statistics and PK teams; identify risks/mitigations and ensure GCP/SOP compliance.