Jobs / United States / Regeneron Pharmaceuticals INC
Clinical Laboratory Project Manager
Regeneron Pharmaceuticals INC · 🇺🇸 3 Locations
Sponsorship verdict
Sponsorship possible
One solid signal, not two — worth applying, and worth asking about sponsorship early.
- Employer is on a government sponsor recordThe US Department of Labor certified 290 H-1B/E-3 labor condition applications for this employer between Oct 2025 and Jun 2026 (latest Jun 2026) — the step every H-1B hire needs first. USCIS also records 40 H-1B approvals in FY2023. Source: LCA disclosure data (US Department of Labor (OFLC)).
- The posting doesn’t mention sponsorshipSilence isn’t a refusal — ask the recruiter before investing much time.
- No salary bar for this routeH-1B has no fixed salary bar: the employer must pay at least the prevailing wage for the role and area. Cap-subject employers enter a lottery weighted by wage level. Source: https://www.federalregister.gov/documents/2025/12/29/2025-23853/weighted-selection-process-for-registrants-and-petitioners-seeking-to-file-cap-subject-h-1b, rules effective 2026-02-27.
- What Regeneron Pharmaceuticals INC paid sponsored hires in similar roles2 certified filings for “Product Manager” (Information Technology Project Managers) in NJ: $181k–$205k, median $193k. Most were filed at wage level IV (100%) — 4 lottery entries, ≈61% projected selection odds for cap-subject employers. Source: US Department of Labor LCA disclosure data (Oct 2025 – Jun 2026).
- Confirmed live todayWhen a source last listed this job as open.
US H-1B: cap-subject employers enter a lottery weighted by wage level — Level I gets 1 entry, Level IV gets 4 (DHS projected selection odds ≈15% at Level I to ≈61% at Level IV). Universities and non-profit research employers are cap-exempt. The $100,000 fee for new petitions from abroad is currently blocked by a court order (appeal pending).
A verdict summarises public evidence; it is not legal advice and never a guarantee — the employer and the immigration authority decide. Sign in to factor in where you can already work.
Or apply yourself on the official page →
Sponsor Radar — Regeneron Pharmaceuticals INC
The US Department of Labor certified 290 H-1B/E-3 labor condition applications for this employer between Oct 2025 and Jun 2026 (latest Jun 2026) — the step every H-1B hire needs first. USCIS also records 40 H-1B approvals in FY2023. Source: LCA disclosure data (US Department of Labor (OFLC)).
Past sponsorship or register membership never guarantees sponsorship for this vacancy or for you. Full Sponsor Radar for Regeneron Pharmaceuticals INC →
About the role
Build Our Future Together The Clinical Lab Project Manager is responsible for program-level oversight of biomarker and clinical laboratory operations within Precision Medicine. The individual provides planning and operational leadership—proactively managing various strategic forums, quality, timelines, vendors, and risk—for the conduct of clinical research studies in accordance with applicable regulations, ICH/GCP, and company Standard Operating Procedures within assigned programs. The role leads strategy, planning, and continuous-improvement efforts for the function and is a member of the Precision Medicine Clinical Laboratory Operations leadership team, interfacing with senior leadership across Global Development. When & where: • Work 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. Oversee portfolio of clinical studies that flow through decision making forums. • 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 ex