Manager Precision Medicine

Job Summary The Manager, Precision Medicine Clinical Laboratory Study Management (CLSM Manager) will lead and develop a team of Clinical Laboratory Study managers (CLSM) for various therapeutic areas including Non‑Immuno‑Oncology (non‑IO). In this role, you will be a key driver of precision medicine operational execution partnering with Precision Medicine Strategy Lead (PMSL), clinical study teams, data management (DM), Samples, Kits, Data, Logistics (SKDL), Clinical Laboratory Study Manager (CLSM), and Clinical Laboratory Project Management (CLPM) groups to deliver high‑quality samples and data. Through strong cross‑functional collaboration and operational excellence, you will help ensure biomarker and non‑biomarker strategies are executed seamlessly, enabling the translation of innovative science to medicines for patients. Key Responsibilities Works with project manager and set‑up manager of central/specialty lab and clinical study team to build lab database to address clinical trial sample collection needs, kits, testing and logistics. Monitors acquisition of clinical trial samples (including human tissue, bone marrow aspirate, whole blood, plasma, serum, etc.) and ensures compliance with ICF permissions. Supports individual clinical study teams as required for all technical and operational sample‑related matters for assigned projects by liaising with internal stakeholders working on ICF and other trial documents impacting samples and testing. Works closely with central lab and/or specialty lab project managers, clinical trial management team, and CRO to ensure samples are collected per protocol and assist with resolving any sample related issues or queries. Oversees study start‑up, closeout and overall life‑cycle activities for assigned studies at central lab/specialty labs to support all samples and testing. Provides input on sample‑related section in clinical trial‑related (e.g. protocols and ICF) and other supporting documents. Works closely with data management lead and SKDL to determine how sample and testing data will be captured, blinded and transferred for clinical trials. Enables transfer of sample/testing data from vendors through development and review of appropriate data transfer specification and related documents in collaboration with SKDL. Provides guidance to clinical teams and clinical sites regarding collection and storage of samples acquired during clinical trials or other human sample acquisition projects. Works with scientists and clinical team to ensure sample collection and usage is in compliance with study protocol and applicable ICF. Day‑to‑Day Activities A typical day may include the following: Works with project manager and set‑up manager of central/specialty lab and clinical study team to build lab database to address clinical trial sample collection needs, kits, testing and logistics; monitors acquisition of clinical trial samples (including human tissue, bone marrow aspirate, whole blood, plasma, serum, etc.) and ensures compliance with ICF permissions; supports individual clinical study teams as required for all technical and operational sample‑related matters for assigned projects by liaising with internal stakeholders working on ICF and other trial documents impacting samples and testing; works closely with central lab and/or specialty lab project managers, clinical trial management team, and CRO to ensure samples are collected per protocol and assist with resolving any sample related issues or queries; oversees study start‑up, closeout and overall life‑cycle activities for assigned studies at central lab/specialty labs to support all samples and testing; provides input on sample‑related section in clinical trial‑related (e.g. protocols and ICF) and other supporting documents; works closely with data management lead and SKDL to determine how sample and testing data will be captured, blinded and transferred for clinical trials; enables transfer of sample/testing data from vendors through development and review of appropriate data transfer specification and related documents in collaboration with SKDL; provides guidance to clinical teams and clinical sites regarding collection and storage of samples acquired during clinical trials or other human sample acquisition projects; works with scientists and clinical team to ensure sample collection and usage is in compliance with study protocol and applicable ICF. Qualifications This role may be for you if: you possess strong leadership tendencies, ability to proactively identify problems, determine resolutions, set priorities, and direct projects and work cross‑functionally to manage expectations with excellent communication and collaborative skills and work well in a team‑based environment. The CLSM Manager will be responsible for day‑to‑day oversight of multiple CLSMs, including responsibility for coaching, mentoring and performance management ensuring applicable key trial level milestones are achieved on schedule. You demonstrate strong leadership skills and possess a high level of emotional intelligence and effectively work collaboratively with colleagues, vendors and internally at Regeneron to ensure program success. To be considered for this role, you must have a bachelor’s degree, minimum of 8 years pharmaceutical experience in matrix interaction preferably in a pharmaceutical or biotech industry, or in academic or governmental cross‑disciplinary teams, minimum of 5 years’ experience with Clinical Trials, focus on clinical sample collection, extensive experience in Clinical laboratory operations, biospecimen logistics, and/or clinical study experience requested. We need a strong understanding of technical, clinical, and strategic aspects of laboratory operations delivery required. We are seeking clinical study knowledge, demonstrated by knowledge in science and technology. Benefits We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels. For additional information about Regeneron benefits in the US, please visit For other countries’ specific benefits, please speak to your recruiter. 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, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company’s business. Equal Opportunity Statement 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, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company’s business. #J-18808-Ljbffr Regeneron Pharmaceuticals, Inc (USA)