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Associate Director, Clinical Supply Chain Planning

Revolution Medicines · Redwood City, California, United States · On-site

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About Revolution Medicines

Backed by GV.

About the role

Collaborating with product leads and study managers, will ensure global clinical demand for RevMed and Non Rev-Med commercial products is accurately reflected within the N-side system on a monthly basis as part of DnOP process. Drive business process standardization, implementation, and training on new processes. Found on 1752vc Careers, the job board for startup and VC roles.

What they're looking for

  • Bachelor’s degree in Supply Chain, Life Sciences, Engineering, Business, or a related discipline, advanced degree preferred
  • Typically 8+ years of relevant experience in pharmaceutical or biotechnology supply chain, including substantial experience supporting clinical-stage programs
  • Demonstrated experience independently managing clinical supply planning for complex, global clinical studies. Oncology experience preferred
  • Strong understanding of clinical development and the clinical supply lifecycle, including forecasting, manufacturing planning, packaging and labeling, distribution, depot management, inventory management, and returns/reconciliation
  • Experience developing demand forecasts and scenario models based on enrollment, dosing, treatment duration, randomization, site activation, and other clinical assumptions
  • N-side forecasting tool experience
More about this role

Revolution Medicines is a global, commercial-state oncology company dedicated to discovering, developing and delivering innovative medicines for patients with RAS-addicted cancers. Leveraging its differentiated RAS(ON) tri-complex inhibitor platform, the company is advancing a broad, integrated portfolio of oral RAS(ON) inhibitors designed to directly target the active, cancer-driving state of RAS. Founded on rigorous scientific inquiry and a willingness to challenge long-held assumptions, Revolution Medicines is committed to changing the trajectory of disease for patients with RAS-addicted cancers worldwide.

Our people are united by a shared way of working: follow the science, challenge assumptions, act with urgency and hold ourselves to a high standard of rigor—all in service of patients.

Collaborating with product leads and study managers, will ensure global clinical demand for RevMed and Non Rev-Med commercial products is accurately reflected within the N-side system on a monthly basis as part of DnOP process.

Drive business process standardization, implementation, and training on new processes.

Lead end-to-end clinical supply planning for assigned clinical programs and...

Read the full posting on Revolution Medicines's site ↗

Supply Chain

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