Associate Director - Study Integration Manager, Data Integration and Automation - Hybrid

Role: Lead study integration for clinical data management, ensuring quality and compliance in trial data components such as eCRFs, integrations, and reports. Responsibilities include developing program plans, managing cross-functional coordination, risk mitigation, change control, and overseeing validation and audit readiness. The role involves direct leadership of complex trials, process improvement initiatives, and team development. Requirements: Bachelor's degree with 8+ years in clinical data management or related fields, including 2 years of people management; or an advanced degree with 4+ years of relevant experience, including 2 years of leadership. High-Value: Experience with clinical trial lifecycle, GxP standards, validation, audit preparation, and data systems integrations; familiarity with automation tools and programming interfaces; strong stakeholder engagement skills. The role supports biopharma development programs likely in clinical phases, with an emphasis on data integrity, quality, and regulatory compliance. Collaboration involves Clinical, DI&A/IT, service providers, and other stakeholders. Work setup: hybrid with 10% travel.