Associate Director, Clinical Supply Chain

Olema Oncology is dedicated to developing better medicines for breast cancer and beyond. Our lead program, palazestrant (OP-1250), is a complete estrogen receptor antagonist (CERAN) currently in development for metastatic breast cancer with blockbuster potential as a monotherapy and in combination in ER+/HER2- metastatic breast cancer.

Our follow-on product candidate, OP-3136, is a potent KAT6 inhibitor with best-in-class potential.   Our scientific breakthroughs are accelerated through the ways in which we fearlessly support, motivate, and challenge one another. At Olema, we know that when we put people first, our work becomes second to none.

If you’re ready to join us at the edge of something unstoppable, let’s make a profound impact together for our patients, for your career, for what’s beyond.  You can view our latest corporate deck and other presentations here.

About The Role

>>>  Associate Director, Clinical Supply Chain  As the Associate Director of Clinical Supply Chain reporting to the Senior Director, Clinical Supply Chain, you will plan, create, implement, build, and optimize the clinical supply chain to ensure uninterrupted and timely clinical drug supply for Olema’s clinical programs.     This role is available in either our San Francisco or Cambridge office and will require about 15% domestic or international travel.

Your work will primarily encompass:   End to End clinical supply chain management    Develop and implement global Clinical Supply Chain strategies   Manage global inventories, shipping, and third-party manufacturers / logistics providers   Develop and manage Interactive Response Technologies (IRT) systems   Oversight packaging, labeling, and distribution activities at multiple vendors   Generate and manage clinical labels   Identify supply chain risks, escalate if needed, and close out risk items   Partner with Clinical Operations to align on assumptions and build clinical supply to meet program demand   Represent Clinical Supply Chain on study execution teams  Knowledge:   Bachelor's degree is required, Master’s degree is preferred    Late phase clinical development and clinical supply chain management   Thorough knowledge of Good Manufacturing Practices (GMP)   Experience:   10+ years of biotechnology/pharmaceutical industry experience in clinical supply chain management   Inventory management and third-party logistics oversight experience   Extensive experience managing forecast demands   Prior experience managing global, large, late-stage studies with standard of care drugs   Strong global shipping and customs experience   Solid experience developing clinical labels   Experience developing IRT specifications   Hands-on experience and troubleshooting proficiency with QMS and purchasing systems   Prior experience in oncology trials using small molecules is preferred    Excellent project management skills   Attributes:   Excellent verbal and written communication and skills   Analytical thinking with problem-solving skills and the ability to adapt to changing priorities and deadlines   A commitment to excellence   Self-motivated and enthusiastic; fast learner who can identify the core project challenges and expeditiously change course as required in a fast-paced organization   Teamwork and collaboration; balances team and individual responsibilities; gives and welcomes feedback; puts success of team above own interests; supports everyone's efforts to succeed; shares expertise with others   Entrepreneurial mindset and the ability to prioritize key work streams and requirements that will change over the near and mid-term   A demonstrated ability to make decisions on incomplete information and in areas where a high degree of professional judgment is required   Be a “difference maker” in terms of one’s professionalism and contributions   Have impeccable professional ethics, integrity and judgment   Be collegial, hard-working, confident, a self-starter and have a passion for results  The base pay range for this position is expected to be $185,000 - $200,000 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-CK1Important Information >>> 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. Fraud Alert:  We are aware of employment scams where individuals pose as representatives of Olema Oncology and make false use of our company name to defraud job seekers. To protect yourself, please note that Olema’s official email addresses end in @olema.com. Our official corporate website is olema.com; our careers page is olema.com/careers; our LinkedIn page is linkedin.com/company/olema-oncology. Please visit these links for official information from Olema.

Communication from any other variant is fraudulent. Olema does not conduct interviews via text message/messaging platforms, will not ask you to download anything as part of your interview, will never request any form of payment, provide upfront payments of any kind, and does not make job offers without an in-person interview.

Olema Pharmaceuticals is a biopharmaceutical company dedicated to developing targeted therapies for women's cancers. With a focus on precision medicine, Olema is committed to advancing innovative treatments that address the unmet medical needs of patients with hormone receptor-positive breast cancer.