Jobs at Regeneron

Lead a regional ophthalmology sales team to meet sales targets, hire/train/coaching staff, ensure compliance, deploy resources using data analysis, build cross-functional partnerships, manage key customer and therapeutic leader relationships, and represent the brand at industry meetings and conferences.

The Regional Director will lead the Rare Neurology Medical Specialist team, ensuring high performance, compliance, and sales growth while managing training, hiring, and budget resources within the Northeast Region.

Field-based account director managing 10-12 academic medical centers to drive launch and commercial performance of a C5 inhibitor for gMG. Responsibilities include formulary strategy, P&T engagement, infusion center education, payer and specialty pharmacy coordination, KOL engagement, CRM-driven analytics, KPI tracking, and cross-functional planning to maximize patient access and revenue. Frequent travel within the assigned Northeast territory required.

The Clinical Imaging Scientific Director will strategize and execute oncology imaging in clinical trials, develop imaging endpoints, and collaborate with teams for effective implementation.

The Associate Director of Thought Leader Liaison in Neurology will engage with key thought leaders, supporting marketing initiatives, coordinating engagements, and ensuring regulatory compliance.

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.

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.

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.

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.

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.

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.