Sr Clinical Supply Operations Specialist

Scorpion Therapeutics; New Jersey; On-site; USD 110,000 - 140,000; Full time

Job summary

Scorpion Therapeutics seeks a Sr. Clinical Supply Operations Specialist to support clinical drug supply and logistics for complex studies, focusing on inventory control, shipment coordination, and regulatory compliance.

The role spans Warren, NJ or Armonk, NY with up to 25% travel. You will lead supply planning, reconcile inventory, manage shipments and temperature excursions, and contribute to regulatory filings.

Qualifications

• BS/BA in a related field with 3+ years in clinical supplies or biopharma operations.
• Strong knowledge of GCP/ICH guidelines and regulatory documentation.
• Proficient in MS Office and data tracking systems.

Responsibilities

• Lead supply planning and inventory reconciliation for complex studies.
• Coordinate shipments and manage temperature excursions.
• Prepare regulatory documentation and support vendor coordination.
• Forecast budgets and participate in continuous improvement initiatives.

Skills

Clinical supply

Inventory management

Regulatory awareness

Communication

Problem-solving

Cross-functional collaboration

Education

BS/BA in related field

Tools

MS Office

Job description

Role

The Sr. Clinical Supply Operations Specialist supports clinical drug supply and logistics for complex studies across multiple therapeutic areas, focusing on inventory management, shipment coordination, and compliance with regulatory standards.

Responsibilities

Responsibilities include supply planning, inventory reconciliation, shipment and temperature excursion management, documentation for regulatory filings, vendor coordination, and budget forecasting. The role may lead short-term projects and participates in continuous improvement initiatives.

Requirements

BS/BA in a related field with at least 3+ years of experience in clinical supplies, QA/regulatory, supply chain, or biopharma research/operations. Skills include knowledge of clinical development processes, GCP/ICH guidelines, proficiency in MS Office, problem-solving, and communication.

Preferred Qualifications

Preferred qualifications include experience with biologics, precision medicine, or manufacturing in a clinical trial context.

High-value Specifics

High-value specifics: supporting highly complex studies with international logistics, compliance with GxP standards, and involvement in regulatory documentation.

Location

Warren, NJ or Armonk, NY, with up to 25% travel. The position involves cross-functional collaboration, adherence to regulatory policies, and working within a fast-paced, science-driven environment.