Senior Clinical Scientist, Immune/Inflammatory Programs

Regeneron Pharmaceuticals, Inc (USA); Village of Tarrytown (NY); Vor Ort; USD 151.000 - 246.000; Vollzeit

Zusammenfassung

Regeneron Pharmaceuticals, Inc. (USA) seeks a Senior Manager in Clinical Sciences to design, execute, and interpret immunology and inflammation studies, partnering with Medical Directors and cross-functional study teams to advance candidates through early and late-phase development.

You will author trial documents, safeguard patient safety, manage risk to study integrity, and represent Clinical Sciences on program teams and safety monitoring boards.

Qualifikationen

• MS/PhD/PharmD in a related scientific field with 8+ years pharma clinical drug development experience.
• Strong knowledge of GCP, ICH guidelines, trial design, and regulatory requirements.
• Excellent medical writing skills and clinical research methodology expertise.
• Experience in Immune/Inflammatory clinical trials preferred.
• Demonstrated success working cross-functionally in a matrix organization.

Aufgaben

• Lead the scientific strategy behind clinical studies from design through execution and reporting.
• Partner with Medical Directors and cross-functional teams to shape protocols, amendments, and study conduct.
• Build deep expertise in disease biology, compound mechanism of action, and the competitive treatment landscape.
• Author and review key trial documents, including expanded synopses, monitoring plans, and study reports.
• Safeguard patient safety through ongoing clinical and medical data review.
• Identify risks to study integrity early and drive practical mitigation strategies.
• Represent Clinical Sciences on program teams, steering committees, and safety monitoring boards.

Kenntnisse

GCP/ICH knowledge

Clinical trial design

Regulatory understanding

Medical writing

Cross-functional collaboration

Ausbildung

MS/PhD/PharmD in a related field

Jobbeschreibung

Regeneron Pharmaceuticals, Inc. (USA) seeks a Senior Manager in Clinical Sciences to design, execute, and interpret immunology and inflammation studies, partnering with Medical Directors and cross-functional study teams to advance candidates through early and late-phase development.

You will author trial documents, safeguard patient safety, manage risk to study integrity, and represent Clinical Sciences on program teams and safety monitoring boards.