Global Clinical Supply Distribution Lead

Exelixis; Alameda (CA); On-site; USD 167,000 - 237,000; Full time

Job summary

Exelixis in Alameda, CA seeks Associate Clinical Supply Distribution Director to lead global logistics for clinical supplies, ensuring uninterrupted site and patient access through depot networks, compliant import/export, and temperature-controlled shipment execution.

You will act as area SME, oversee budgeting, data management, vendor performance, and cross-functional collaboration with clinical operations and project teams, while maintaining regulatory and GMP standards.

Qualifications

• Experience in international pharmaceutical logistics and supply chain.
• Experience in the pharmaceutical and biotech industries.
• Strong knowledge of GMP regulations.

Responsibilities

• Oversight of logistics and distribution of clinical supplies with GxP compliance.
• Ensure regulatory compliance and documentation including customs.
• Partner with Trade Compliance to manage VAT/tax and INCO terms.
• Process owner for site-by-site drug product shipments and temperature control.
• Maintain distribution data for budget creation and adherence.
• Liaise with clinical operations and project teams on issues and resolutions.
• Develop country requirement database for import/export considerations.
• Identify vendor performance improvements within governance and KPIs.

Skills

Clinical supply distribution

GxP compliance

Regulatory knowledge

Vendor management

Budgeting

Customs & import/export

HTS knowledge

US Customs reporting

MS Office

Education

BS/BA in related field

MS/MA in related field

Equivalent combination

Job description

Exelixis in Alameda, CA seeks Associate Clinical Supply Distribution Director to lead global logistics for clinical supplies, ensuring uninterrupted site and patient access through depot networks, compliant import/export, and temperature-controlled shipment execution.

You will act as area SME, oversee budgeting, data management, vendor performance, and cross-functional collaboration with clinical operations and project teams, while maintaining regulatory and GMP standards.