Senior Manager, Clinical Scientist, Immunology
Regeneron
August 19, 2026
On-site
Tarrytown, NY
Clinical Research and Development
Responsibilities:
- 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 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.
- Champion consistent, high-quality data review practices across assigned studies.
Qualifications:
- MS, PhD, or PharmD in a related scientific field.
- 8+ years of pharmaceutical clinical drug development experience (other levels considered based on experience).
Required/Preferred Skills:
- Proven knowledge of GCP, ICH guidelines, clinical trial design, and regulatory requirements.
- Strong medical writing skills and clinical research methodology expertise.
- Experience in Immune/Inflammatory clinical trials (preferred).
- Demonstrated success working cross-functionally in a matrix organization.
Application Instructions:
- Apply now.
- 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 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.
- Champion consistent, high-quality data review practices across assigned studies.
Qualifications:
- MS, PhD, or PharmD in a related scientific field.
- 8+ years of pharmaceutical clinical drug development experience (other levels considered based on experience).
Required/Preferred Skills:
- Proven knowledge of GCP, ICH guidelines, clinical trial design, and regulatory requirements.
- Strong medical writing skills and clinical research methodology expertise.
- Experience in Immune/Inflammatory clinical trials (preferred).
- Demonstrated success working cross-functionally in a matrix organization.
Application Instructions:
- Apply now.