Jobs at Regeneron

Authors nonclinical PK/PD study reports, eCTD summaries, Investigator’s Brochure content, and integrated regulatory narratives. Collaborates with pharmacology and translational teams to interpret data, coordinate reviews, manage timelines, and ensure consistent messaging across drug development programs. Supports process improvements through authoring guidance, workflow optimization, and AI-enabled writing and quality-control solutions while serving as the scientific writing lead for assigned programs.

Drafts and manages Clinical Pharmacology and Clinical Bioanalysis submission reports across clinical development phases and therapeutic areas. Leads document meetings, review timelines, cross-functional collaboration, data consistency checks, and template maintenance. The role also supports digital solutions for content generation and requires strong scientific writing, communication, attention to detail, and familiarity with biotech or pharmaceutical development.

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.

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.

The Associate Director of Pathology supports drug efficacy and safety studies, provides histopathology evaluation, mentors junior Pathologists, and collaborates on scientific teams to advance therapeutics.