Manage HCP engagement and contracting operations, providing training and compliance guidance while optimizing processes in the pharmaceutical sector.

Oversee the Review Committee Team’s daily operations, ensuring MLR review compliance of promotional materials for Regeneron products across multiple regions. Manage meetings, guide promotional sponsors, collaborate with teams on Veeva PromoMats, and participate in quality assurance checks.

The Senior Clinical Study Lead manages global execution of complex clinical trials, ensuring compliance, budget management, and process improvement while leading teams and overseeing vendor engagement.

The Director, Program Operations Leader oversees clinical operations for trials, ensuring quality, timelines, and budgets are met. Responsibilities include management of staff, budget oversight, stakeholder communication, and operational insights on clinical program development.

The Senior Clinical Study Lead is responsible for the global execution of complex clinical trials, ensuring compliance, managing study timelines and budgets, overseeing vendor engagements, and leading the clinical study teams.

Regulatory Affairs Manager role involves developing EU regulatory strategies, overseeing clinical study submissions, and ensuring compliance with EU legislation.