Cytokinetics

Associate Director, Clinical Supply Planning

Cytokinetics$195K — $227K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • MS or BS in chemistry, pharmaceutics, or a related discipline; advanced degree preferred.
  • 8+ years manufacturing experience in the biotech/pharmaceutical industry.
  • 5+ years of experience in Operations Management.
  • Strong understanding of clinical supply systems (e.g., IRT, ERP).
  • Experience with data visualization tools like Tableau and Power BI.

Responsibilities

  • Develop and maintain end-to-end supply plans for clinical programs.
  • Translate clinical development forecasts into executable supply strategies.
  • Lead cross-functional scenario planning and risk assessments.
  • Manage global clinical supply programs across all clinical development phases.
  • Establish best practices and drive process standardization across studies.

Benefits

  • Hybrid work model to support work-life balance.
  • Cross-functional collaboration opportunities for career growth.
  • Focus on innovation and continuous improvement in supply chain processes.
  • Diverse workplace that values different backgrounds and experiences.
Full Job Description
The Associate Director, Clinical Supply Chain, will develop and formulate supply chain strategies, meet project deliverables, solve business problems and drive improvements within Global Clinical Supply Chain (GCSC), as well as the Cytokinetics enterprise. This position includes all elements of the clinical supply planning from translating protocol design into executable demand forecasts, through manufacturing to the ultimate distribution and inventory management of clinical supplies at clinical sites worldwide. This role ensures the timely, compliant delivery of high-quality clinical trial materials and investigational medicinal products through cross-functional collaboration, efficient resource management, and vendor oversight. The incumbent will also drive innovation and continuous improvement within clinical supply chain processes while ensuring alignment across the organization, as well as maintaining regulatory compliance to meet corporate objectives.

Key Responsibilities:

Supply Chain Planning
  • Develop and maintain end-to-end supply plans for clinical programs, including demand forecasting, production planning, and inventory strategies across depots and external CDMOs.
  • Translate clinical development forecasts into executable supply strategies that align with CMC, Clinical Operations, Quality, and Regulatory milestones.
  • Lead cross-functional scenario planning and risk assessments to ensure uninterrupted supply throughout the clinical development lifecycle.
  • Lead Global Clinical Supply Chain planning activities within the operating model, including CDOP (Clinical Development Operations Planning) and Clinical Supply & Operations Planning.

Supply Chain Execution
  • Demonstrated experience managing global clinical supply programs across all phases of clinical development.
  • Proven ability to lead cross-functional planning activities and align supply plans with Clinical Operations, CMC, Quality, Regulatory, and external partners.
  • Strong vendor management experience, including oversight of CDMOs, depots, IRT providers, logistics providers, and other clinical supply partners.
  • Proven track record of leading process improvement initiatives and implementing scalable solutions.
  • Establishes best practices and drives process standardization across studies, programs, and vendors.

Systems & Analytics
  • Experience utilizing and supporting clinical supply systems (e.g., IRT, APS, ERP) to enable planning and operational excellence.
  • Strong analytical capabilities with experience using KPIs, dashboards, and performance metrics to support decision making.
  • Experience with data visualization and analytics tools such as Tableau, Power BI, and Excel to support performance monitoring and business insights.
  • Ability to identify trends, risks, and opportunities through data analysis and translate findings into actionable recommendations.
Skills:
  • Strong leadership and business acumen, with a track record of driving improvements cross-functionally with an entrepreneurial mindset.
  • Exceptional problem-solving, decision-making, and project management abilities.
  • Excellent written and verbal communication skills, with the ability to effectively present complex information to diverse audiences.
  • Advanced proficiency in change management and cross-functional collaboration.
Preferred:
  • Experience with oral solid dose and associated manufacturing/packaging and regulatory documentation.
  • Familiarity with IRT/IWRS/ERP systems capabilities and their operational requirements.
Qualifications:
  • MS or BS in chemistry, pharmaceutics or a related discipline; advanced degree preferred.
  • 8+ years manufacturing experience in biotech/pharmaceutical industry.
  • 5+ years Operations Management experience

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Pay Range:

In the U.S., the hiring pay range for fully qualified candidates is $195,390 - $227,955 per year. The base pay actually offered will take into account internal equity and also may vary depending on the candidate's geographic region, job-related knowledge, skills, and experience among other factors.

Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you.

About Cytokinetics

Cytokinetics is a late-stage biopharmaceutical company focused on discovering, developing, and commercializing muscle activators and inhibitors as potential treatments for debilitating diseases in which muscle performance is compromised and/or declining. The company was founded in 1997 and is headquartered in South San Francisco, California.
Learn more about Cytokinetics
Size
253 employees
Market Cap
$4.4 billion
Industry
Net Income
-$127.2 million
5 Year Trend
-7.9%
Revenue
$55.8 million
NASDAQ

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