Jobs at Regeneron

Field-based account director responsible for launching and driving commercial performance of a C5 inhibitor across ~10-12 AMCs and neuromuscular centers. Manage formulary access, P&T engagements, infusion center pull-through, KOL relationships, account planning, CRM analytics, and cross-functional coordination. Track KPIs, prepare business reviews, and travel frequently within an assigned Mountain West territory to maximize patient access and revenue.

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.

Field-based, non-sales liaison responsible for engaging hematology thought leaders, sharing clinical and product information, gathering insights, coordinating executive engagements, supporting speaker bureaus and advisory boards, and maintaining compliant relationships. The role collaborates with Marketing, Sales, Medical Affairs, Market Access, and leadership teams across a Northeast territory, requiring 60%–80% travel.

Supports Global Development quality system governance, quality event oversight, metrics and trend reporting, root cause investigations, CAPA development, procedural reviews, and continuous improvement. The role collaborates with quality stakeholders, facilitates governance meetings, presents quality system data, supports regulatory inspections, delivers training, and provides subject matter expertise in GCP and GVP quality management.

Lead end-to-end, risk-based GCP audits of investigator sites, vendors, license partners, and internal processes; schedule, conduct, report, and follow up on audits; apply FDA, EU, and ICH E6 R3 regulations to resolve compliance issues; develop audit strategies; support inspections and cross-functional compliance projects; mentor and onboard GDQA staff.