Senior Manager, Clinical Lab Project Management

BioSpace; United States; Hybrid; USD 134,000 - 219,000; Full time

Job summary

Regeneron seeks a Senior Manager, Precision Medicine Clinical Laboratory Operations to oversee clinical lab projects across therapeutic areas. You will partner with PM, trial teams, and global colleagues to keep study deliverables on track and manage risk.

The role supports early and late-stage programs, with a focus on biomarker delivery, lab operations, and cross-functional leadership within a matrix environment.

Qualifications

• Experience leading clinical laboratory operations and portfolios.
• Strong project management and risk assessment capabilities.
• Proven ability to collaborate across functional teams in biotech/pharma.

Responsibilities

• Manage clinical laboratory portfolio and review timelines and risks.
• Serve as SME on central and specialty laboratory processes.
• Maintain biomarker strategy delivery schedules and mitigation plans.
• Oversee testing/data generation schedules and portfolio objectives.
• Build strong, cross-functional relationships with trial teams and Global Development.

Skills

Clinical laboratory operations

Project management

Risk management

Cross-functional collaboration

Communication

Education

Bachelor's degree

Master's degree preferred

Tools

CTMS

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, Precision Medicine Clinical Laboratory Operations who will be responsible for Clinical Laboratory Project & Program management across various therapeutic areas, working closely with the Director, Precision Medicine Clinical Laboratory Operations and key cross‑functional collaborators. The primary role will be to keep laboratory deliverables across the portfolio on track, ensuring that study start timelines are met, and provide risk management. This will be done in collaboration with Precision Medicine Strategy Leads, Clinical Trial Management, Clinical Laboratory Operations Management, Global Development colleagues, and central and specialty testing laboratories to support early and late‑stage programs within our pipeline.

When & Where

This role can be based remotely (in the US) or sit on‑site in our Warren, NJ or Armonk, NY office. If on‑site, the role would be expected to be on‑site four days per week.

Discover Your Role

• Perform clinical laboratory portfolio management for Regeneron clinical trials and review clinical laboratory operations timelines and risks and be able to manage and communicate risks and ensure study starts and data delivery are aligned with expectations
• Be a subject matter expert on central and specialty laboratory processes and leverage this knowledge to be a trusted collaborator and ensure clinical laboratory deliverables
• Keep biomarker strategy delivery schedules for clinical development programs and studies on track, identifying and tracking risks and decisions, creating mitigation plans
• Manage clinical laboratory operations goals, including progress, schedules of testing/data generation across the portfolio with clear objectives and deadlines
• Manage strong relationships and trust with internal and cross functional partners, including Precision Medicine Clinical Lab Study Management, Precision Medicine Strategy Leads and others within Global Development to manage and implement program level clinical laboratory management
• Demonstrate relevant knowledge and understanding of clinical laboratory trial requirements on the program and implement operational decisions. Ensure the laboratory portion of the studies are harmonized for assigned program from onset to final delivery
• Be viewed as an operational subject matter expert to effectively communicate with clinical study teams on laboratory program direction. Demonstrate authority for the studies related to the program
• Create and communicate enhancements to Clinical Laboratory Project Management and connections through the matrix environment, design and develop processes to address identified gaps

This Role Requires

• Bachelors degree required, Masters degree preferred.
• Minimum of 10 years experience 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.

At Regeneron, 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.

Salary Range (annually)

$134,400.00 - $219,200.00

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. 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.

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.