About this role
Clinical Laboratory Project Manager
Location: Armonk, NY or Warren, NJ or Remote, USA Hybrid: 4 days per week on site
Discover your role: Maintain a program-level overview of clinical laboratory status and issues; proactively communicate progress, risks, issues, or changes that may impact quality, timelines, and/or budget, and provide program-level updates to stakeholders as requested. Oversee clinical laboratory timelines across the assigned program(s); review plans and provide clinical laboratory operations decision making per the clinical laboratory strategy for early lab engagement, study start-up, and conduct phases, ensuring study starts and data delivery are aligned with decision making. Ensure timely delivery of operational deliverables and accountability for consistency of process and approach across clinical study teams within programs. Lead and facilitate strategic forums, planning, and operations efforts for the function—including objective and goal setting, organizational planning for vendor visits, lab leadership, and cross-functional business reviews for assigned program(s). Support functional laboratory strategy and allocation, translational meetings, IVDR committee workflows, budget management for the program(s), liaising with cross-functional leadership and finance, and review key metrics and Key Performance Indicators to track progress and drive action plans to address issues. Build trusted relationships with internal and cross-functional partners and senior leadership—including Precision Medicine Clinical Lab Study Management, Precision Medicine Strategy Leads, and Global Development—and communicate program direction to internal teams, providing frequent executive summaries while remaining able to dive into detail when required. Bridge laboratory clinical trial operations across research, translational medicine teams and tech centers at Regeneron, managing timelines for lab delivery in clinical trials and other human-sample projects to ensure seamless execution and adherence to commitments. Drive decision making and lead program direction, delivery, and implementation of strategic change and continuous-improvement initiatives for Precision Medicine Operations; including but not limited to samples/assays within the protocols, timeline management for operations, translational medicine initiatives. Incorporate industry best practices and innovation to keep operations current and practical. This role requires:
- Bachelor’s degree and 10+ years of relevant industry experience, preferably in a pharmaceutical or biotech environment or in academic or governmental cross-disciplinary teams.
- Experience with working alongside clinical trials—with a focus on continuous improvement and clinical laboratory operations decision making and alignment.
- Demonstrated process improvement and experience in strategic planning, vendor strategy and governance, risk mitigation, leading internal and external meetings, and complex operational solutioning is essential.
- PMLabOps
As part of the recruitment process, Regeneron may conduct background checks in accordance with local laws. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief, sex, sexual orientation, gender identity or expression, marital or civil partnership status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, military or veteran status, or any other characteristic protected by law. Salary ranges and compensation details are provided during the recruitment process. Regeneron offers a competitive total rewards package, which may include bonuses, equity, retirement benefits, health and wellness programs, and paid time off. For additional information about Regeneron benefits, please visit the career site. If you have any questions, please speak with your recruiter.