Local Study Associate Director CAR-T

Experteer Overview

In this role you drive country‑level CAR‑T study delivery, translating complex strategies into operational excellence. You lead cross‑functional collaboration to activate sites, safeguard quality, and maintain data integrity across milestones. Based in Milan, you balance speed with regulatory readiness in a fast‑moving environment. You will coach teams, strengthen site partnerships, and sharpen activation timelines to bring transformative therapies to patients sooner. This is a hands‑on leadership role with a clear impact on study delivery and patient access.

Retribuzione / Benefits

• Lead the Local Study Team, establish an operating rhythm, optimize performance within budget, ensure governance and run high‑value meetings
• Translate protocol into country execution plans, craft monitoring strategies, identify and select sites, and secure on‑time submissions for rapid activation
• Lead country feasibility assessments, identify high‑potential sites, evaluate recruitment opportunities, and shape execution plans with investigators
• Conduct co‑monitoring, review monitoring outputs for trends, oversee audits, and drive corrective actions to stay inspection‑ready
• Maintain complete, accurate documentation, keep systems current, and prepare for final archiving to protect data integrity
• Collaborate with CRAs, Investigators and Regulatory Affairs; provide progress updates and manage risks
• Onboard and coach new team members; drive process improvements to reduce cycle times and scale best practices
• Support regional initiatives and uphold company values to harmonize ways of working beyond a single study

Responsabilità

• Proven ability to lead a Local Study Team, optimize performance, ensure compliance, run meetings, and manage budgets
• Experience delivering study commitments with monitoring plans, site selection, and timely document submissions
• Experience performing co‑monitoring, reviewing monitoring reports, and overseeing audit activities
• Ability to ensure document completeness, maintain study information in required systems, and prepare for final archiving
• Strong collaboration with CRAs, Investigators and Regulatory Affairs with regular progress updates
• Experience training new team members and contributing to process improvements
• Commitment to company values and willingness to support regional initiatives

Requisiti fondamentali

• annual target bonus
• participation bonus
• sales incentives
• wellbeing benefits
• insurance
• psychological support