Director, Clinical Supply Chain
Location: Cambridge, MA and San Francisco, CA, United States
Employer: Olema Oncology
About the Role >>> Director, Clinical Supply Chain
As the Director of Clinical Supply Chain reporting to the Senior Director, Clinical Supply Chain, you will have oversight of aspects of the clinical supply chain to ensure uninterrupted and timely clinical drug supply for all Olema’s clinical programs. This will include supply chain development; global supply demand and inventory management; operations; and oversight of label development, and package manufacturing, and finished product distribution.
This hands-on role requires an independent self-starer with extensive experience on clinical supply chain management. The role will be based out of our San Francisco or our Cambridge office and require occasional travel.
Your work will primarily encompass:
-Provide technical, functional, and project leadership on clinical supply chain development, supply manufacturing, and CDMO management.
-Develop and implement global Clinical Supply Chain strategies and deliver clinical supplies for all phases of clinical development.
-Manage global inventories, shipping, and third-party manufacturers / logistics providers.
-Work collaboratively with CMC, Clinical Operation, Quality Assurance, Regulatory, Finance and Legal.
-Identify supply chain risks, escalate if needed, and close out risk items.
-Stay current with state-of-the art approaches and applicable global regulations and industry standards.
Ideal Candidate Profile >>> Late Phase Clinical Supply Knowledge
A love of challenging, important work. We are a pragmatic team, driven to imagine and develop meaningful therapies for improving lives. All employees within our company play a unique and crucial role in our success, both in accomplishing our mission and building a positive company culture. As such, we are looking for someone with the right combination of knowledge, experience, and attributes for this role.
Knowledge
-Bachelor’s degree is required, Master’s degree is preferred.
-Late phase clinical development and global clinical supply chain management experience is required.
-Thorough knowledge of Good Manufacturing Practices (GMP).
Experience:
-12+ years of biotechnology/pharmaceutical industry experience, with 8+ years in clinical supply chain management.
-Expertise in late-phase clinical supply chain development and management, inventory management and third-party logistics oversight.
-Extensive experience managing forecast demands and inventories.
-Strong experience in clinical label development, global shipping and customs.
-Excellent project management skills.
-3+ years of people management experience.
-Demonstrated successful partnerships with the Clinical Operations team to deliver in the late phase of drug development.
-Experience scaling a department/business function by implementing structure and processes in a way that can support consistent growth, is highly preferred.
Attributes:
-High level of curiosity and intelligence; highly analytical.
-Self-starter with great initiative who’s able to work independently and deliver on follow-through.
-Positive can-do attitude.
-Good communication and interpersonal skills; able to work cross-functionally.
-Driven to meet goals.
-Able to multi-task and shift priorities rapidly to meet tight deadlines.
-Aspires to the highest level of scientific and ethical standards.
-Keen to improve processes and overcome inefficiencies.
How to Apply:
Please apply through Olema’s job page. Here are the links for each region:
San Francisco, CA: https://job-boards.greenhouse.io/olema/jobs/5403278004
Cambridge, MA: https://job-boards.greenhouse.io/olema/jobs/5403279004