The role involves managing drug supply activities for clinical studies to ensure accurate and continuous supply to patients while reducing risk and minimizing waste
Job Summary
The role involves managing drug supply activities for clinical studies to ensure accurate and continuous supply to patients while reducing risk and minimizing waste.
Candidates must possess working knowledge of clinical supply best practices, IRT systems, and experience within a cGMP environment.
The company offers a comprehensive benefits package including medical, dental, vision, 401(k), life insurance, and opportunities for equity ownership.
Matching Summary
The role involves managing drug supply activities for clinical studies to ensure accurate and continuous supply to patients while reducing risk and minimizing waste.
Salary
Base: $131,800.00 - $176,800.00 annually; Bonus/Equity: Eligible for annual bonus plan and discretionary equity awards; Benefits: Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, Wellness
Skills & Requirements
Must-have
7 years progressive supply chain experience
GMP environment knowledge
IRT systems expertise
Clinical trial material planning
Label and pack management
Nice-to-have
Collaborative spirit with stakeholders
Process improvement leadership
Risk mitigation strategy development
Cross-functional project coordination
Key Requirements
Bachelor's or Master's degree in Business Administration or related field
Minimum 7 years of progressive supply chain experience
Experience in biotech, pharmaceutical, or CRO industry