Full-Time

Associate Director

Posted on 4/19/2024

Revolution Medicines

Revolution Medicines

201-500 employees

Develops precision oncology therapies

Biotechnology

Compensation Overview

$160,000 - $200,000Annually

+ Equity + Learning and Development Opportunities

Senior

San Carlos, CA, USA

Requirements
  • Sc. or M.Sc. in scientific field with 8+ years of experience in pharmaceutical strategic sourcing and/or supply chain.
  • Experience working with domestic and international CRDMOs.
  • Experience developing, negotiating, and executing clinical or commercial supply and/or quality agreements.
  • Experience managing both strategic and tactical/operational projects.
  • Working knowledge of and experience in clinical manufacturing, regulatory, QA, and cGMP requirements for small molecules.
  • Working knowledge of small molecule drug development and commercialization, including raw material and starting material sourcing, API/drug substance manufacturing, process development, process engineering, and process characterization.
  • Working knowledge of pharma end-to-end supply chain.
  • Strong negotiation skills.
  • Solid project management, facilitation, and problem solving skills.
  • Solid organizational and time management skills.
  • Effective, open, and transparent communication skills (verbal and written)
  • 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.
Responsibilities
  • Serve as Revolution Medicines’ primary business operation lead and business and project management interface between internal PDM functions and CRDMOs for drug product and finished product.
  • Establish and maintain mutually beneficial long-term business relations with CRDMOs.
  • Lead contract negotiations in close collaboration with cross-functional team. Ensure best terms and conditions.
  • Support preparation and execution of CRDMOs business reviews with PDM senior management.
  • Support development and implementation of outsourcing strategies for PDM.
  • Drive the selection process for CRDMOs in collaboration with technical SMEs.
  • Ensure projects/programs meet desired results, compliance, speed, quality, and cost.
  • Support development of scope of work (SOW) in close collaboration with technical SMEs.
  • Support cross-functional CRDMO management activities, covering all aspects such as business needs identification, market screening, contracting, vendor qualification and set-up, compliant delivery of services, and discontinuation.
  • Support management of CRDMO budget, purchase orders, and invoices.
  • Work with PDM senior management and cross-functional teams to assess and manage supplier performance through use of personal influence, internal business review meetings, and/or joint governance meetings.
  • Identify and deliver on cost savings opportunities.

Revolution Medicines specializes in developing precision oncology therapies, particularly RAS(ON) inhibitors and RAS Companion inhibitors, with their lead product candidate, RMC-4630, currently in a Phase 1/2 clinical program targeting specific oncogenic mutations in various tumor types. The company's main focus is on developing these therapies to target specific oncogenic mutations in different tumor types, utilizing precision oncology technologies.

Company Stage

IPO

Total Funding

$1.3B

Headquarters

Redwood City, California

Founded

2014

Growth & Insights
Headcount

6 month growth

22%

1 year growth

50%

2 year growth

103%