Clinical Supply Chain Lead - Global Trials

Eikon; Millbrae (CA); On-site; USD 170,000 - 205,000; Full time

Benefits offered by this job

401k with company match

Medical, dental and vision insurance

Mental health benefits

Paid time off and holidays

Equity compensation

Daily on-site lunch program

Job summary

Eikon Therapeutics, Millbrae, CA, is seeking an Associate Director of Clinical Supply Chain to lead the end-to-end supply for investigational products across global trials. You will translate study information into demand plans and manage supplies at CMOs, depots, and sites, while aligning with CMC and Study Management teams.

You will collaborate across Clinical Operations, QA, and Regulatory, ensuring compliant, timely supply execution and risk mitigation.

Qualifications

• Requires 10+ years with a Bachelor's degree or 8+ years with a post-graduate degree.
• Clinical supply chain experience is a must, with exposure to manufacturing, quality, and regulatory.
• Strong collaboration with internal and external stakeholders across Clinical Operations, QA, CMC, Regulatory, and CMOs.

Responsibilities

• Translate clinical trial assumptions into drug forecasts and supply plans.
• Lead clinical supply chain execution and support study teams as needed.
• Serve as liaison to Clinical Operations customers and strategic supply-related issues.
• Plan and maintain IP supply project plans and complex study forecasts.
• Manage study budget and timely payment of CMOs.
• Oversee packaging/labeling and final drug release processes.

Skills

Clinical supply chain

Cross-functional collaboration

Regulatory/GxP knowledge

Communication & organizational skills

Project planning

Negotiation & stakeholder management

Problem solving

Education

Bachelor's degree

Post-graduate degree

Tools

MS Excel

PowerPoint

MS Project

Office Timeline

Job description

Eikon Therapeutics, Millbrae, CA, is seeking an Associate Director of Clinical Supply Chain to lead the end-to-end supply for investigational products across global trials. You will translate study information into demand plans and manage supplies at CMOs, depots, and sites, while aligning with CMC and Study Management teams.

You will collaborate across Clinical Operations, QA, and Regulatory, ensuring compliant, timely supply execution and risk mitigation.