Senior Clinical Supply & Logistics Lead

Regeneron Pharmaceuticals, Inc; New Jersey; On-site; USD 84,000 - 137,000; Full time

Job summary

Regeneron Pharmaceuticals, Inc. is seeking a Senior Clinical Supply Operations Specialist to support the IP distribution, ancillary supplies, and comparator procurement across multiple studies.

Located in Warren, NJ or Armonk, NY with up to 25% travel, the role involves leading complex supply planning and ensuring regulatory compliance. The successful candidate will have a Fundamentals in the clinical drug development process and ICH/GCP knowledge, plus strong MS Word/Excel skills and a

Qualifications

• BS/BA degree required with 3+ years in Clinical Supplies, QA/Regulatory, Precision Medicine, Supply Chain, Manufacturing or equivalent biopharma experience.
• Fundamental knowledge of the clinical drug development process and trial methodology.
• Familiarity with ICH/GCP and regulatory guidelines/directives.
• Proficiency in MS Word and Excel.
• Strong problem solving, time management, communication, and collaboration skills.

Responsibilities

• IP Supply & Inventory Planning including ARRD and reconciliation activities.
• IP Shipments management, depot transfers, and temperature excursion oversight.
• eTMF management: EDL creation and document control; QA/QP release tasks.
• Ancillary Supply planning, including procurement support, shipping and logistics.
• Comparator planning and market intelligence; manage document storage and related processes.
• Financial forecasting, budgeting, planning, and demand updates.

Skills

MS Word

MS Excel

Problem Solving

Time Management

Ambiguity Tolerance

Action Oriented

Adaptability

Collaboration

Communication

Detail Orientation

Education

BS/BA degree in related field

3+ years in Clinical Supplies/QA/Regulatory/Supply Chain/Manufacturing or related biopharma

Tools

MS Word

MS Excel

Job description

Regeneron Pharmaceuticals, Inc. is seeking a Senior Clinical Supply Operations Specialist to support the IP distribution, ancillary supplies, and comparator procurement across multiple studies.

Located in Warren, NJ or Armonk, NY with up to 25% travel, the role involves leading complex supply planning and ensuring regulatory compliance. The successful candidate will have a Fundamentals in the clinical drug development process and ICH/GCP knowledge, plus strong MS Word/Excel skills and a