Senior Clinical Supply & Logistics Lead

Regeneron Pharmaceuticals, Inc (USA); Kentucky; On-site; USD 84,000 - 137,000; Full time

Benefits offered by this job

Annual bonuses

Equity awards

401(k) company match

Health and wellness programs

Paid time off

Job summary

Regeneron Pharmaceuticals, Inc (USA) seeks a Sr. Clinical Supply Operations Specialist to support IP distribution, ancillary supplies, and comparator procurement across multiple studies.

Based in Warren, NJ or Armonk, NY, you’ll lead IP shipments, inventory planning, and eTMF documentation, coordinating with CROs and internal partners to ensure on‑time, compliant delivery. We require a BS/BA and 3+ years in clinical supplies, QA/regulatory, or related biopharma fields; strong MS Word/Excel

Qualifications

• Fundamental knowledge of the clinical drug development process and trial methodology.
• Fundamental knowledge of ICH/GCP and regulatory guidelines.
• Proficient in MS Word & Excel; strong problem solving and time management.

Responsibilities

• IP Supply & Inventory Planning: ARRD, batch status, and inventory maintenance.
• IP Shipments: system/non-system shipments, depot transfers, temperature control.
• IP Supply Monitoring & eTMF: EDL creation, document management, QA/QP release.
• Ancillary Supply & Inventory: procurement support, vendor RFI, shipping requirements.
• Comparator Planning: market intelligence, quotes, requisitions, documentation.

Skills

MS Word

Excel

Proactive problem solving

Time management

Communication

Detail oriented

Collaborates effectively

Organized

Education

BS/BA degree in related field

Job description

Regeneron Pharmaceuticals, Inc (USA) seeks a Sr. Clinical Supply Operations Specialist to support IP distribution, ancillary supplies, and comparator procurement across multiple studies.

Based in Warren, NJ or Armonk, NY, you’ll lead IP shipments, inventory planning, and eTMF documentation, coordinating with CROs and internal partners to ensure on‑time, compliant delivery. We require a BS/BA and 3+ years in clinical supplies, QA/regulatory, or related biopharma fields; strong MS Word/Excel