Associate Manager, Clinical Laboratory Study Management

Build our future together At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. As an Associate Manager, Precision Medicine Clinical Laboratory Study Management, you will play a critical role in advancing precision medicine capabilities across multiple therapeutic areas, including Non-Immuno-Oncology. Partnering with cross-functional teams across clinical development, precision medicine, data management, and laboratory operations, you will help ensure the successful delivery of high-quality biospecimens and laboratory data that inform clinical decision-making. Through operational excellence, leadership, and collaboration, you will support the execution of biomarker and non-biomarker strategies that accelerate the development of innovative therapies for patients worldwide. When & where Location: Office-based in Tarrytown, NY; Armonk, NY; or Warren, NJ On-site expectation: 4 days per week for office-based employees Discover your role Lead and support Clinical Laboratory Study Managers (CLSMs) and external functional service provider resources across assigned therapeutic programs and studies. Partner with clinical study teams, precision medicine leaders, laboratory vendors, CROs, and internal stakeholders to execute sample collection, testing, and data delivery strategies. Oversee operational planning and lifecycle activities for central and specialty laboratory services, including study start-up, execution, and close-out. Monitor clinical sample acquisition and handling activities, ensuring compliance with informed consent requirements and protocol-defined procedures. Provide subject matter expertise on laboratory operations, biospecimen management, and sample-related clinical trial processes within assigned therapeutic areas. Support vendor selection activities by contributing to RFP development, bid evaluations, and scope of work assessments related to sample testing and laboratory services. Collaborate with data management and sample logistics teams to establish processes for laboratory data capture, transfer, blinding, and reporting. Identify operational risks, resolve sample-related issues, and help ensure critical study milestones and laboratory deliverables are achieved on schedule. This role requires Bachelor's degree required. Minimum 6-8 years of pharmaceutical, biotechnology, academic, or governmental cross-functional experience required. Minimum 5 years of clinical trial experience with a focus on clinical sample collection. Extensive experience in clinical laboratory operations, biospecimen logistics, and/or clinical study management. Strong understanding of technical, clinical, and strategic aspects of laboratory operations delivery. Demonstrated knowledge of clinical research, scientific principles, and emerging technologies supporting clinical studies. Proven ability to manage stakeholders, lead internal and external meetings, and develop practical solutions to complex operational challenges. #PMLabOps Does this sound like you? Apply now to take your first step towards living the Regeneron Way! 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.   Where necessary,