Senior Supply Chain Specialist, Clinical Logistics
Gilead Sciences
Summary
The Senior Supply Chain Specialist, Clinical Logistics plays a critical role in supporting global clinical development programs by ensuring the reliable, compliant, and efficient movement of clinical materials across a global clinical supply network. Working closely with Clinical Supply Chain, Quality, Regulatory Affairs, Trade Compliance, contract manufacturing organizations, and third-party logistics providers, this role supports clinical supply operations across a complex and highly regulated environment.
Job description
Key Responsibilities
- Execute end-to-end logistics activities supporting the movement of clinical materials across domestic and international supply networks, including transportation planning, shipment coordination, and distribution activities.
- Establish and maintain transportation lanes that support reliable, compliant, and efficient shipment execution.
- Coordinate and monitor clinical drug shipments to ensure timely delivery, temperature compliance, and chain-of-custody integrity.
- Support logistics operations in accordance with GDP, GMP, company procedures, and applicable regulatory requirements while partnering with Quality, Regulatory Affairs, and Trade Compliance teams to ensure required documentation and shipment controls are maintained.
- Maintain accurate clinical supply information and execute inventory-related activities, including monitoring inventory status, investigating discrepancies, and processing inventory transactions.
- Serve as a primary logistics point of contact for internal stakeholders, contract manufacturing organizations, third-party logistics providers, and other external business partners.
- Build and maintain effective cross-functional partnerships to support supply continuity and clinical study startup activities.
- Identify and mitigate logistics risks that may impact supply, service, quality, or compliance.
- Support the investigation and resolution of shipment exceptions, delays, temperature excursions, and other logistics-related issues.
- Drive continuous improvement initiatives that enhance logistics operations, compliance, service levels, and data quality.
- Review, author, and maintain departmental standard operating procedures and work instructions while supporting training and compliance with established processes.
- Facilitate communication of operational updates, process changes, corrective actions, and other logistics-related activities across stakeholders.
Basic Qualifications
Bachelor's Degree and Five Years' Experience OR Master's Degree and Three Years' Experience
Preferred Qualifications
- Experience supporting pharmaceutical, biotechnology, or regulated healthcare supply chain operations.
- Knowledge of GDP and GMP operating environments.
- Experience supporting domestic and international shipment activities.
- Experience with cold-chain logistics or temperature-controlled shipment operations.
- Experience working with contract manufacturing organizations, third-party logistics providers, or similar logistics partners.
- Ability to collaborate across internal functions and external partners supporting regulated logistics operations.
- Demonstrated ownership, accountability, and sense of urgency in a fast-paced environment.
Requirements
- Bachelor's Degree and Five Years' Experience OR Master's Degree and Three Years' Experience
- Experience supporting pharmaceutical, biotechnology, or regulated healthcare supply chain operations.
- Knowledge of GDP and GMP operating environments.
- Experience supporting domestic and international shipment activities.
- Experience with cold-chain logistics or temperature-controlled shipment operations.
- Experience working with contract manufacturing organizations, third-party logistics providers, or similar logistics partners.
- Ability to collaborate across internal functions and external partners supporting regulated logistics operations.
- Demonstrated ownership, accountability, and sense of urgency in a fast-paced environment.
Benefits
- Medical, Dental & Vision
- Life Insurance
- Paid Time Off
- Annual Bonus
- Stock-based Long-term Incentives
Company overview
Gilead Sciences, Inc. is a leading American biopharmaceutical company headquartered in Foster City, California, that specializes in researching, developing, and commercializing innovative medicines for life-threatening diseases. Founded in 1987, Gilead has grown into a global healthcare leader with approximately 17,600 employees worldwide. The company's primary therapeutic focus areas include HIV/AIDS, viral hepatitis (hepatitis B and C), oncology, inflammation, and respiratory diseases. Gilead is renowned for its groundbreaking antiviral therapies, including Sovaldi and Harvoni for hepatitis C, and its comprehensive portfolio of HIV treatments such as Truvada, Atripla, and Biktarvy. The company also developed Veklury (remdesivir) for COVID-19 treatment. Gilead operates as a publicly traded company on the NASDAQ (GILD) and is a component of both the Nasdaq-100 and S&P 100 indices. Through strategic acquisitions like Kite Pharma and Immunomedics, Gilead has expanded into cell therapy and oncology, demonstrating its commitment to advancing medical science and improving patient outcomes globally.