Director, Clinical Supply Chain

This is a fully remote position, open to applicants in United States.

📋 Description

• Take ownership of the long-term clinical supply strategy for BBOT’s oncology initiatives.

• Ensure that sourcing, production, and distribution align with pipeline priorities.

• Collaborate with clinical operations, regulatory, and manufacturing teams to synchronize trial requirements and supply timelines.

• Identify potential supply risks and formulate mitigation strategies.

• Source commercial comparators, including conducting due diligence and coordinating with vendors.

• Develop and manage Excel-based supply-and-demand models.

• Conduct scenario and sensitivity analyses to inform planning, budgeting, and resource allocation.

• Maintain the IRT system for supply configuration and tracking purposes.

• Oversee inventory management, expiry tracking, and batch traceability across various sites and depots.

• Assist in the setup and configuration of clinical supply chain systems, including IRT user acceptance testing and release.

• Manage label creation and prepare clinical supply documentation for regulatory submissions.

• Support the supply budget and procurement processes for clinical supplies and services.

• Ensure compliance with regulatory and country-specific requirements.

• Collaborate with quality teams on batch release, QP support, deviation management, and audit preparedness.

• Assist in the selection and qualification of suppliers and negotiate vendor contracts.

• Manage relationships with manufacturers, packaging providers, and logistics companies to guarantee timely and compliant delivery of clinical trial materials.

⛳️ Requirements

• Bachelor's degree in Supply Chain Management, Life Sciences, or a related discipline.

• At least 10 years of experience in clinical supply chain within pharma or biotech, with a minimum of 5 years in a leadership role.

• Experience in small to medium-sized biotech firms is highly preferred.

• Comprehensive knowledge of clinical trial operations, cGMP/GDP regulations, and global clinical supply chain best practices.

• Proficiency in advanced Excel and supply modeling techniques.

• Ability to forecast and manage supply, inventory, and risk across multiple global oncology trials.

• Strong skills in negotiation, vendor management, and contract oversight.

• Exceptional communication, interpersonal, and leadership abilities, with the capability to influence at the executive level.

• Ability to excel in a fast-paced, growing environment and adapt swiftly as priorities shift.

🏝️ Benefits

• Fully remote work environment.

• Occasional domestic and international travel.