Jobs at Regeneron

Lead hiring, developing, and retaining a Hematology medical specialist sales team across the Great Plains to drive Multiple Myeloma bispecific antibody sales. Ensure targets are met or exceeded, manage regional budget and resources, analyze sales/customer data, coordinate cross-functional activities, ensure compliance and training, represent the brand at industry events, and travel extensively to support regional performance.

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.

Lead and develop a Hematology field sales team across the Mid Atlantic to drive sales of a Multiple Myeloma bispecific antibody. Hire, train, evaluate, and retain staff; set and manage budgets; ensure compliance; analyze sales/customer data; coordinate cross-functionally; represent the brand at industry events; and meet/exceed regional sales objectives.

Lead and manage pharmacoepidemiology projects to generate real-world evidence and fulfill regulatory post-marketing study requirements. Serve as subject-matter expert across cross-functional teams, design and analyze epidemiologic studies using external databases, support risk management, regulatory filings, safety surveillance, and process improvements.

Lead clinical data management activities for complex studies: oversee eCRF/database design, data quality, CRO/vendor oversight, data transfers, SAE/AE reconciliation, coding, database lock/archiving, and inspection readiness. Ensure timelines, metrics, and process improvements across study lifecycle.

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 national hematology oncology commercial strategy and Field teams to prepare for launch of two bispecific biologics. Hire, train, and develop Regional Directors and medical specialists; drive revenue, budgets, compliance, and cross-functional alignment with Marketing, Market Access, Medical Affairs, and Commercial Operations.

The Regional Director for Rare Neurology oversees recruiting and leading a sales team, develops sales strategies, ensures compliance, manages budgets, and builds relationships in the Rare Neurology market.

Lead and manage a global GCP audit program: hire and develop staff, plan and conduct internal and external GxP/GCP audits, provide compliance input cross-functionally, drive process improvements, support regulatory inspections, and deliver training to Global Development QA and partner teams.

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.