ESSENTIAL JOB FUNCTIONS:
Responsible for leading and developing the clinical drug supply strategy, planning and management of all supply chain activities required to support global Phase I - III clinical studies including forecasting, supply planning, IRT configuration, inventory management and CMO management.
Collaborate with the Clinical Development and Clinical Operations teams from protocol development through final study design to have an in-depth understanding of the clinical study requirements and assumptions needed to set up the supply chain required to support the execution of the study and develop the IP forecast.
Participate in Clinical Sub Team (CST) meetings, Study Team meetings, Project Team meetings and present Supply Chain updates as required to the Kura cross-functional team.
Develop an expert-level understanding of the IRT system used to manage site activation, IP site shipments, monitor patient enrollment, patient visits, determine trends and execute adjustments.
Manage extensive internal and external touchpoints and maintain close communication and collaboration to ensure adequate clinical drug supply for multiple global clinical trials while ensuring compliance with cGMP and global regulatory requirements.
Responsible for providing commercial supply chain support in collaboration with the Manufacturing, Quality and the Commercial team including serialization expertise, as well as the release and distribution of commercial product from 3PL to authorized trading partners in compliance with the Drug Supply Chain Security Act (DSCSA).
Participate in the creation and maintenance of clinical and commercial SOP's and Work Instructions and related documentation.
Lead continuous improvement initiatives in collaboration with the IMSC team, as well as cross-functional partners to document, standardize and streamline core supply chain processes supporting Kura's clinical programs, as well as the commercial supply chain.
Support financial planning for global clinical studies including budgeting, forecasting and strategic planning activities.
---
JOB SPECIFICATIONS:
Technical degree or equivalent (BS/MS), preferably in Supply Chain or IT
8-10 years pharmaceutical/biotechnology supply chain planning and forecasting experience, preferably in a manufacturing or commercial environment
3-5 years of leadership experience in pharmaceutical/biotechnology industry with a proven track record of leading teams and delivering results
Experience managing complex global supply chain operations including vendor partnerships, contract negotiations, while ensuring compliance with cGMP regulations and requirements
Experience collaborating with Manufacturing, Quality and CMO's including providing a 12 - 24 month rolling forecast of drug product requirements, managing production schedules and coordinating FG deliveries
Comprehensive knowledge of CMC requirement/activities including development, validation, regulatory and quality requirements and timelines
The base range for a Director is $202,000 - $235,672 per year. Individual pay may vary based on additional factors, including, and without limitation, job-related skills, experience, work location, and relevant education or training. Kuras compensation package also includes generous benefits, equity, and participation in an annual target bonus.
#LI-RM1