Director, Clinical Supply Chain - Comparators/External Collaborations

Revolution Medicines; San Francisco (CA); On-site; USD 211,000 - 264,000; Full time

Benefits offered by this job

Competitive cash compensation

Robust equity awards

Strong benefits

Learning and development opportunities

Job summary

A clinical oncology company is seeking a Director of Clinical Supply Chain to manage comparator sourcing and ensure compliance across their clinical portfolio. The ideal candidate should have over 10 years of experience in Clinical Supply Chain operations, particularly in global oncology trials. This hands-on leadership role involves collaborating with clinical program leads, mitigating supply risks, and maintaining vendor partnerships. Salary range is competitive and reflects local market conditions, with a base pay of $211,000 - $264,000.

Qualifications

• 10+ years of Clinical Supply Chain operations experience.
• Strong knowledge of global pharmaceutical procurement.
• Excellent cross-functional leadership skills.

Responsibilities

• Develop Comparator Sourcing governing structure for clinical supply needs.
• Collaborate with clinical supply leads for product sourcing needs.
• Ensure compliance with GxP and global trade regulations.

Skills

Clinical Supply Chain operations experience

Oncology trials

Global pharmaceutical procurement

Vendor management

Strategic thinking

Cross-functional leadership

Education

Bachelor’s degree in supply chain, Business, Engineering or Life Sciences

Master’s degree (MS, MBA)

CPIM/CSCP certifications

Job description

Overview

Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The company’s R&D pipeline comprises RAS(ON) inhibitors designed to suppress diverse oncogenic variants of RAS proteins. The company’s RAS(ON) inhibitors daraxonrasib (RMC-6236), elironrasib (RMC-6291), zoldonrasib (RMC-9805), and RMC-5127 are in clinical development. As a new member of the Revolution Medicines team, you will join other outstanding professionals in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway.

The Opportunity

The Director, Clinical Supply Chain – Comparators and External Collaborations is a hands-on leadership role responsible for building scalable processes for comparator sourcing needs across the clinical portfolio, ensuring uninterrupted, compliant and cost-effective supply. The Director will also lead clinical supply activities related to external strategic partnerships and clinical collaborations.

Responsibilities

• Develop and lead Comparator Sourcing governing structure and operating model for the Clinical Supply Chain group focusing on overall demand and supply planning across all programs.
• Collaborate with clinical supply program and study leads to identify comparator and external collaboration product needs. Formalize a sourcing/delivery plan as part of the Demand & Operations process (D&OP) and develop processes to communicate status to all internal and external stakeholders.
• Assess and mitigate supply risks, including but not limited to potential shortages, vendor capacity, regulatory requirements, financial targets.
• Partner with PDM Strategic Sourcing group to develop and maintain partnerships with comparator sourcing vendors, support sourcing agreement negotiations and plans for sourcing diversification to build high-performance, resilient global supply networks.
• Ensure all externally sourced products comply with applicable GxP and global trade regulations.
• Accountable for comparator sourcing financial budgets and budget adherence across the global development portfolio.
• Develop and maintain comparator products master profiles, lead processes to resolve any product related issues, including but not limited to temperature excursions, deviations, product complaints.
• Develop and maintain applicable KPI’s.
• Review and evaluate applicable supply agreements.
• Partner with Alliance Management and internal stakeholders to provide supply related requirements applicable to external collaboration agreements and associated clinical studies.

Qualifications

Required Skills, Experience and Education

• 10+ years of Clinical Supply Chain operations experience. Experience with global oncology trials across all phases of development.
• Strong knowledge of global pharmaceutical procurement and contract/supply agreement execution. Strong at comparator planning and sourcing strategies.
• Bachelor’s degree in supply chain, Business, Engineering or Life Sciences. Master’s degree (MS, MBA). CPIM/CSCP certifications a plus.
• Strong knowledge and experience with end-to-end supply chain and demand/supply planning.
• Strong vendor management and contract oversight skills.
• Strategic thinker with strong tactical execution.
• Excellent cross-functional leadership skills with effective communication skills.

Preferred Skills

• Proven leadership in working with matrixed teams.
• Knowledge and experience with outsourced manufacturing operations and strategic sourcing.
• Effective, open and transparent communication skills (verbal and written). Strong analytical, communication and executive level reporting skills.
• Capable of working on multiple projects/tasks and able to meet timelines.
• Self-starter with a high-level of comfort with ambiguity and complexity and the ability to multi-task while consistently delivering quality results.
• Team-oriented, progressive thinker who enjoys participating in an innovative and creative work environment.

The base pay salary range for this full-time position for candidates working onsite at our headquarters in Redwood City, CA is listed below. The range displayed on each job posting is intended to be the base pay salary range for an individual working onsite in Redwood City and will be adjusted for the local market a candidate is based in. Our base pay salary ranges are determined by role, level, and location. Individual base pay salary is determined by multiple factors, including job-related skills, experience, market dynamics, and relevant education or training.

Please note that base pay salary range is one part of the overall total rewards program at RevMed, which includes competitive cash compensation, robust equity awards, strong benefits, and significant learning and development opportunities.

Revolution Medicines is an equal opportunity employer and prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital status, medical condition, and veteran status.

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Base Pay Salary Range

$211,000 - $264,000 USD

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