Associate Manager, Clinical Laboratory Study Management

Regeneron Pharmaceuticals, Inc (USA); United States; Hybrid; USD 98,000 - 160,000; Full time

Benefits offered by this job

Annual bonuses

Equity awards

Pension or retirement benefits

401(k) company match

Health and wellness programs

Fitness centers

Insurance benefits

Paid time off

Family support benefits

Job summary

Regeneron Pharmaceuticals, Inc. is seeking an Associate Manager for Precision Medicine Clinical Laboratory Study Management.

You will lead CLSMs, coordinate with clinical teams, precision medicine leaders, laboratories, CROs, and internal stakeholders to execute sample collection, testing, and data delivery strategies. You will oversee laboratory service startup, execution, and close-out, monitor sample acquisition, ensure informed consent and protocol compliance, and manage risks to keep

Qualifications

• Bachelor's degree required.
• 6–8 years of pharmaceutical/biotech cross-functional experience.
• 5+ years of clinical trial experience focused on clinical sample collection.
• Extensive experience in clinical laboratory operations, biospecimen logistics, and/or clinical study management.
• Proven ability to manage stakeholders and lead meetings with internal and external partners.

Responsibilities

• Lead and support CLSMs and external resources across therapeutic programs.
• Partner with clinical study teams, precision medicine leaders, labs, CROs and internal stakeholders to execute sample collection, testing and data delivery strategies.
• Oversee startup, execution and close-out of central and specialty laboratory services.
• Identify operational risks and resolve sample-related issues to ensure milestones and deliverables are met.

Skills

Cross-functional collaboration

Laboratory operations

Biospecimen logistics

Clinical trial experience

Vendor management

Data management

Education

Bachelor's degree

Job description

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.

Location

Remote within the United States or office-based in Tarrytown, NY; Armonk, NY; or Warren, NJ

Work model

Remote or hybrid 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.

Requirements

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.

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, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits.

Salaries and Compensation

Salary Range (annually) $98,100.00 - $160,100.00

For jobs in Canada: this posting is for an existing position.

Benefits and Compensation

• annual bonuses or other incentive plans
• equity awards
• pension or retirement benefits
• 401(k) company match
• health and wellness programs
• fitness centers
• insurance benefits (e.g. medical, dental, vision, life and disability)
• paid time off
• family support benefits

Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other locations, additional information will be provided during the recruitment process.

Regeneron is a leading biotechnology company that invents life-transforming medicines for people with serious diseases. Founded and led for over 30 years by physician-scientists, our unique ability to repeatedly and consistently translate science into medicine has led to nine FDA-approved treatments and numerous product candidates in development, almost all of which were homegrown in our laboratories. Our medicines and pipeline are designed to help patients with eye diseases, allergic and inflammatory diseases, cancer, cardiovascular and metabolic diseases, neurology, infectious diseases and rare diseases.

Regeneron is also proud of award winning culture of innovation, being recognized as a Great Place to Work in 2021, Fast Company's Best Workplace for Innovators in 2020, and Forbes JUST companies in 2020, among others.