Revolution Medicines
Senior Director, Clinical Supply Chain
Revolution Medicines, Redwood City, California, United States, 94061
Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers. The company’s R&D pipeline comprises RAS(ON) Inhibitors designed to suppress diverse oncogenic variants of RAS proteins, and RAS Companion Inhibitors for use in combination treatment strategies. 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:Playing a critical role within the Pharmaceutical Development and Manufacturing (PDM) organization, the position will be responsible for leading a team to plan and deliver clinical supplies to support RevMed’s clinical development programs.
Responsibilities:
Lead a team to plan and deliver on-time, compliant clinical supply per the clinical development plan.
Collaborate with cross-functional teams (i.e. Clinical Operations, QA, PDM, and Regulatory) to proactively identify and mitigate potential risks to the continued advancement of the clinical programs.
Serve as the clinical supply lead for assigned program(s) and develop/manage the clinical supply plan.
Lead and manage clinical supply and logistics activities, including but not limited to demand forecasting and supply planning, IRT start-up and maintenance, label generation and approval, packaging and labeling operations, release and distribution, expiry extension, cold chain management, and inventory management.
Author, review, and/or approve related clinical and technical documents, including but not limited to: clinical label text, clinical/master batch record, clinical trial protocol, pharmacy manual, IND, IMPD, and NDA.
Lead vendor identification, selection, onboarding, and management for combo agent/comparator sourcing and secondary packaging and distribution.
Serve as a subject matter expert and develop continuous improvement plans for clinical supply GMP, GDP, and business processes.
Required Experience, Skills, and Education:
B.S. or M.S. in scientific fields with 15+ years of experience in clinical supply chain and logistics.
5+ years of experience building and/or managing a clinical supply chain team.
Strong experience managing clinical supply activities for global phase 3, randomized, oncology clinical trials.
Working knowledge of import and export laws and processes.
Working knowledge of pharmaceutical drug product development and manufacturing.
Solid organizational and time management skills.
Effective, open, and transparent communication skills (verbal and written).
Preferred Skills:
Capable of working on multiple projects/tasks and able to meet timelines.
Team-oriented, progressive thinker who enjoys participating in an innovative and creative work environment.
The base salary range for this full-time position is $235,000 to $281,000 for candidates based at our headquarters in Redwood City, CA. The range displayed on each job posting is intended to be the minimum and maximum salary for the position in Redwood City and will be adjusted for the local market a candidate is based. Our salary ranges are determined by role, level, and location. Individual pay is determined by multiple factors, including job-related skills, experience, market dynamics, and relevant education or training.
Please note that base salary 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.
Revolution Medicines takes protection and security of personal data very seriously and respects your right to privacy while using our website and when contacting us by email or phone. We will only collect, process and use any personal data that you provide to us in accordance with our CCPA Notice and Privacy Policy. For additional information, please contact privacy@revmed.com.
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The Opportunity:Playing a critical role within the Pharmaceutical Development and Manufacturing (PDM) organization, the position will be responsible for leading a team to plan and deliver clinical supplies to support RevMed’s clinical development programs.
Responsibilities:
Lead a team to plan and deliver on-time, compliant clinical supply per the clinical development plan.
Collaborate with cross-functional teams (i.e. Clinical Operations, QA, PDM, and Regulatory) to proactively identify and mitigate potential risks to the continued advancement of the clinical programs.
Serve as the clinical supply lead for assigned program(s) and develop/manage the clinical supply plan.
Lead and manage clinical supply and logistics activities, including but not limited to demand forecasting and supply planning, IRT start-up and maintenance, label generation and approval, packaging and labeling operations, release and distribution, expiry extension, cold chain management, and inventory management.
Author, review, and/or approve related clinical and technical documents, including but not limited to: clinical label text, clinical/master batch record, clinical trial protocol, pharmacy manual, IND, IMPD, and NDA.
Lead vendor identification, selection, onboarding, and management for combo agent/comparator sourcing and secondary packaging and distribution.
Serve as a subject matter expert and develop continuous improvement plans for clinical supply GMP, GDP, and business processes.
Required Experience, Skills, and Education:
B.S. or M.S. in scientific fields with 15+ years of experience in clinical supply chain and logistics.
5+ years of experience building and/or managing a clinical supply chain team.
Strong experience managing clinical supply activities for global phase 3, randomized, oncology clinical trials.
Working knowledge of import and export laws and processes.
Working knowledge of pharmaceutical drug product development and manufacturing.
Solid organizational and time management skills.
Effective, open, and transparent communication skills (verbal and written).
Preferred Skills:
Capable of working on multiple projects/tasks and able to meet timelines.
Team-oriented, progressive thinker who enjoys participating in an innovative and creative work environment.
The base salary range for this full-time position is $235,000 to $281,000 for candidates based at our headquarters in Redwood City, CA. The range displayed on each job posting is intended to be the minimum and maximum salary for the position in Redwood City and will be adjusted for the local market a candidate is based. Our salary ranges are determined by role, level, and location. Individual pay is determined by multiple factors, including job-related skills, experience, market dynamics, and relevant education or training.
Please note that base salary 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.
Revolution Medicines takes protection and security of personal data very seriously and respects your right to privacy while using our website and when contacting us by email or phone. We will only collect, process and use any personal data that you provide to us in accordance with our CCPA Notice and Privacy Policy. For additional information, please contact privacy@revmed.com.
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