Teams at Regeneron

Leads field-based, non-sales engagement with oncology thought leaders across the Northeast and Great Lakes. Builds strategic relationships, gathers insights, supports speaker bureau and advisory board initiatives, coordinates executive engagements, translates national strategies into regional execution, and ensures compliance with company policies and industry regulations. Requires pharmaceutical marketing expertise, oncology experience, and at least 10 years of relevant experience.

Leads end-to-end, risk-based Good Clinical Practice audits across internal and external global development activities. Responsibilities include planning and conducting process, site, vendor, and partner audits; reporting findings; driving remediation and process improvements; interpreting regulations; supporting regulatory inspections; and representing Quality Assurance on compliance initiatives. The role requires extensive GCP auditing experience, strong knowledge of FDA, EU, and ICH requirements, senior stakeholder leadership, and 30–40% domestic and international travel.

The Associate Director, Government Pricing oversees compliance with pricing regulations, including submitting reports, analyzing pricing trends, and communicating with internal teams. Responsibilities also include monitoring pricing legislation and performing detailed calculations to ensure accurate submissions to government agencies.