Director, Clinical Supplies

Scorpion Therapeutics; Hampton (NJ); On-site; USD 150,000 - 210,000; Full time

Job summary

Scorpion Therapeutics seeks a Director of Clinical Supplies to oversee labeling, packaging, and distribution of clinical trial materials through third-party CSPs for global studies. The role ensures uninterrupted supply, manages CSP relationships, and controls budgets in compliance with GMP and clinical standards.

Primary responsibilities include forecasting, quoting, inventory management via IRT systems, deviation support, and collaboration with Clinical Operations to align supplies with trial

Qualifications

• Bachelor's or Master's in Engineering, Biological Sciences, or Business.
• 10+ years in clinical study product supply management.
• 3-5 years managing third-party providers.
• Project Management Certification preferred.
• Proficiency in IRT systems, MS Office, and project tools.

Responsibilities

• Direct forecasting, quoting, and monitoring of supply chain activities
• Manage inventory via IRT systems
• Support deviations and investigations
• Oversee budgets, expenditures, and performance
• Collaborate with Clinical Operations to align supplies with trial protocols
• Provide forecasts for current and future studies

Skills

Supply chain management

Education

Bachelor's or Master's in Engineering, Biological Sciences, or Business

Tools

IRT systems

MS Office

Project tools

Job description

Role: Director of Clinical Supplies overseeing the labeling, packaging, and distribution of clinical trial materials through third-party CSPs for global trials. Main objectives include ensuring uninterrupted supply, managing CSP relationships, and controlling budgets in compliance with GMP and clinical standards.

Responsibilities:

• direct forecasting, quoting, and monitoring of supply chain activities
• manage inventory via IRT systems
• support deviations and investigations
• oversee budgets, expenditures, and performance
• collaborate with Clinical Operations to align supplies with trial protocols
• provide forecasts for current and future studies

Qualifications:

• Bachelor's or Master's in Engineering, Biological Sciences, or Business
• 10+ years in clinical study product supply management
• 3-5 years managing third-party providers
• Project Management Certification preferred
• proficiency in IRT systems, MS Office, and project tools

High-Value:

• experience with global clinical trial supply, GMP/GDP compliance, supply chain logistics, and budget management
• familiarity with clinical development processes

Work setup and travel details are not specified.