Olema Oncology is a cancer medicines company dedicated to impacting breast cancer and beyond. Our lead program, palazestrant (OP-1250), is a differentiated oral medicine known as a complete estrogen receptor antagonist (CERAN) initially in development for metastatic breast cancer. Our pipeline also includes OP-3136, a potent, selective oral inhibitor of the KAT6 pathway. At Olema, we are building a focused team committed to our mission with intention and clarity. Working alongside a talented passionate group of leaders and advisors, we strive to create better medicines that aim to help patients feel better, longer. For more information, visit us at
www.olema.com.
About the Role
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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
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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.
The base pay range for this position is expected to be $220,000 - $230,000 annually, however the base pay offered may vary depending on location, market, job related knowledge, skills and capabilities, and experience. The total compensation package for this position also includes equity, bonus, and benefits.#LI-CK1
Important Information
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We provide equal opportunity to all employees and applicants for employment and believe that great ideas and discoveries come from a mix of expertise, background, and experience. Olema is building a culture where the value of difference is celebrated.We offer a competitive compensation and benefits package, seeking to provide an open, flexible, and friendly work environment to empower employees and provide them with a platform to develop their long-term careers. A Summary of Benefits is available for all applicants.Please note: Olema doesn’t accept agency resumes and is not responsible for any fees related to unsolicited resumes.
Thank you.
Additional Note/Fraud Alert: Olema will not conduct interviews via text message or messaging platforms and will not ask you to download anything as part of your interview. Though we use third party tools to help with advertising our jobs,
please be vigilant in checking that the communication is in fact coming from Olema.
