Director, Clinical Supply Chain

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Job Summary

About IDEAYA Biosciences: IDEAYA is a precision medicine oncology company committed to the discovery, development, and commercialization of transformative therapies for cancer. Our approach integrates expertise in small-molecule drug discovery, structural biology and bioinformatics with robust internal capabilities in identifying and validating translational biomarkers to develop tailored, potentially first-in-class targeted therapies aligned to the genetic drivers of disease. We have built a deep pipeline of product candidates focused on synthetic lethality and antibody-drug conjugates, or ADCs, for molecularly defined solid tumor indications.

Our mission is to bring forth the next wave of precision oncology therapies that are more selective, more effective, and deeply personalized with the goal of altering the course of disease and improving clinical outcomes for patients with cancer.

When you're at IDEAYA, you will be in the midst of brilliant minds working on precision medicine therapies to help cancer patients. We are passionate and committed about being on the forefront of oncology medicine, which means we all have a high internal drive that is at the very core of every person  are inquisitive, ask deep questions, and are data-driven innovators who like to collaborate and use team work to move science forward.

For more information, please see

Location
:
South San Francisco, CA.

Position Summary

We are seeking an experienced, strategic, resourceful, and highly motivated Director, Clinical Supply Chain. This role requires an individual with demonstrated ability to operate effectively in a fast-paced and evolving environment, engage cross-functionally across departments, and communicate clearly and proactively across internal and external stakeholders. The ideal candidate will be a collaborative leader and critical thinker who can operate with autonomy, manage complex drug supply chains, and translate clinical development needs into actionable supply strategies.

This individual will manage a team responsible for the timely provision of clinical trial material (CTM) for all clinical trials of IDEAYA programs and will oversee vendor relationships, ensure compliance with global regulatory standards, and champion efficient processes to support the successful execution of global clinical trials. The successful candidate will be responsible for but not limited to those activities listed below.

This position is based in our South San Francisco headquarter offices and required to be onsite four days per week per our company policy.

Reporting to:
Vice President, Clinical and Commercial Supply Chain

Job Description

What you’ll do:

Clinical Trial Supply Management (General)

• Manage a team of Clinical Supply Chain professionals to ensure that all IDEAYA clinical programs are continuously supplied with CTM.
• Working with Supply Chain Leadership, implement a Clinical S&OP Process to ensure organization wide alignment on the CTM requirements.
• Proactively manage study supply forecasts and inventory levels across depots and sites to prevent shortages or overages.
• Develop sourcing strategies for commercial comparator or adjunctive supplies, ensuring timely and cost-effective delivery to support all IDEAYA clinical programs.
• Develop Inventory Management process to ensure compliant and timely reporting of global clinical inventory levels.
• Interpret and advise on clinical trial protocols for study supply requirements and identify risks and develop mitigation strategies.
• Develop study specific Pharmacy Manuals and supply related training/instructional materials (i.e., Investigator Meeting and Site Initiation Visit slides, Dosing Cards, Diaries, etc.).
• Ensure appropriate documentation of Investigational Product (IP) supply activities is provided to clinical trial teams for the Trial Master File.
• Participate in relevant team meetings providing clinical supply status reports and support.
• Establish and document the Supply Chain for each project as applicable to scope.
• Handle temperature excursion investigations, product complaints, expiry management, and re-labeling as needed.
• Ensure expiry extensions are…