About this opportunity
Regeneron Pharmaceuticals, Inc lists this Senior Manager GCP Quality opportunity in armonk, New York. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Build our future together:
At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager, GCP Quality Management - Global Development to join our Global Development Quality team, supporting our global clinical development organisation in a hybrid work model. In this role, you will lead risk-based quality management across clinical trials while collaborating with study teams, clinical functions, contract research organisations, and quality colleagues. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.
When & where:
Multiple locations are being considered for this role (Hybrid)
Discover your role:
Lead risk-based quality management across assigned clinical trials
Drive protocol-stage Quality Risk Assessment and Control Tracker activities under ICH E6 R3
Manage quality issues, audit responses, corrective actions, preventive actions, and trend analysis
Partner with study leads, monitoring teams, and contract research organisations on site risks
Escalate significant quality events and trends to Executive Quality Leadership
Support inspection readiness, responses, and follow-up actions across relevant functions
Manage onboarding, development goals, coaching, performance discussions, and team administration
You champion quality, integrity, continuous learning, and trusted partnerships
This role requires:
Bachelor’s degree and eight years’ relevant healthcare or pharmaceutical industry experience
Quality, compliance, clinical development, Good Clinical Practice, or Good Pharmacovigilance Practice experience
Advanced risk-based quality management, risk assessment, and compliance knowledge
Experience managing complex issues, regulatory inspections, and inspection readiness
Subject matter expert, process owner, training, presentation, and staff management experience
Process improvement, project management, prioritisation, and time management skills
Advanced Microsoft Outlook, Word, Excel, and PowerPoint skills
Strong communication, collaboration
Does this sound like you? We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.
For additional information about Regeneron benefits in the U.S., please visit
Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.
As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.
For jobs in Canada: this posting is for an existing position.
Salary Range (annually)
$134,400.00 - $219,200.00
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Worksite address
armonk, NY, 10504, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.