Jobs / United States / Regeneron Pharmaceuticals INC
Sr Clinical Supply Operations Specialist
Regeneron Pharmaceuticals INC · 🇺🇸 Warren
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 roles1 certified filing for “Clinical Supply Operations Specialist” (Logisticians) in NJ: $90k–$90k, median $90k. Most were filed at wage level II (100%) — 2 lottery entries, ≈31% 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.
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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: At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. The Sr. Clinical Supply Operations Specialist provides support to the Clinical Drug Supply & Logistics group in the Investigational Product (IP) distribution process, ancillary supplies process and comparator procurement process, for one or more molecules across multiple Therapeutic areas supporting highly complex studies as well as long-term departmental and cross-functional projects and on-going continuous improvement initiatives. May lead short-term projects. Activities are performed on time, within budget and with good quality, in compliance with Regulatory Authorities’ regulations / guidelines and Regeneron Standard Operating Procedures (SOPs) / Work Practice Documents (WPDs). This role applies to internally sourced studies and/or CRO/Partnered studies. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide. When & where: Location: Warren, NJ or Armonk, NY Travel percentage: Up to 25% Discover your role Solve complex problems, and initiate completion of the following items within broadly defined practices and policies including selecting methods, techniques, and evaluation criteria for obtaining results related to: • IP Supply & Inventory Planning o Accountability, Reconciliation, Returns & Destruction (ARRD) o Internal System Management including lot creation, batch status, and inventory maintenance o Assessment and Oversight activities (risks, stocking levels, trends) • IP Shipments o System and Non-system generated Shipments o Depot transfers o Temperature Excursion Management • IP Supply Monitoring & Activity Documentation (Electronic Trial Master File - eTMF) o Expected Document List (EDL) creation o eTMF Document Management per regulatory requirements o QA/QP Release Management o Pack-and-label kit and sequence reconciliation o Inspection Readiness activities o IRT management activities including IRT Alert management and UAT activities o Suspected Serious Non-Compliance support • Ancillary Supply & Inventory Planning/Management o Procurement support (Includes Work Order Management) o Vendor RFI support o Supply Planning & Inventory Management o Ancillary Supply Plan creation o Shipping & Logistics (Includes International Logistics requirements for Ancillaries) o Shipping & logistics activities o Temperature Excursions o Lot management o eTMF activities o ARRD activities • Comparator Planning & Management o Market Intelligence Reports o Quote/PO/Requisition Process Support o IMN Creation o Document Storage o Temperature Excursions • Financial Forecasting, Budgeting & Planning o Forecast Submissions o Order Ticket Entry o Demand Updates Work is performed under general direction and reviewed upon completion for adequacy in meeting objectives. Candidate is expected to participate in determining objectives of assignment and be able to plan schedules and arrange own activities in accomplishing objectives. Candidate will represent CDSL as a prime contact on contracts or projects. He/She will interact with senior internal and external personnel on significant matters often requiring coordination between organizations. JOB REQUIREMENTS: Fundamental knowledge of the clinical drug development process and clinical trial methodology including the inner-workings of cross-functional partners. Fundamental knowledge of International Council of Harmonization (ICH) / Good Clinical Practices (GCP) & regulatory guidelines/directives · Proficient in MS Word & Excel · Efficient Problem S