Sr. Manager, Supply Chain Planning

At Corcept Therapeutics, we believe the potential impact of cortisol modulation on the future of health has long gone overlooked. That is why for twenty-five years we have pushed the boundaries of what is possible, driven by fiercely independent science, open collaboration and the curiosity to follow the data wherever it leads.

Our company is committed to building a culture that values diverse perspectives and the unique contributions of every employee. Our vibrant community is made up of over 300 people—medical practitioners, scientists, and industry professionals—all with the shared goal of advancing the science of cortisol modulation to treat serious disease.

Our work has uncovered over 1000 proprietary selective cortisol modulators, including our marketed product, Korlym^® (mifepristone), the first treatment available for those living with Cushing’s syndrome, a life-threatening condition caused by excess cortisol activity. Today, we have a unique opportunity to revolutionize the treatment of severe endocrine, oncology, metabolism and neurology disorders and aim to deliver better outcomes for the people affected by them.

As Sr. Manager, Supply Chain Planning, you will be responsible for developing end to end supply plans to ensure continuous drug supply for Corcept’s global clinical trials.  This position will report to the Sr. Director, Supply Chain. 

Essential Duties and Responsibilities:

• Develop supply plans for all Corcept clinical studies
• Perform scenario planning to support decision-making
• Provide clinical supply and risk mitigation recommendations
• Oversee inventory management of study drug and comparators at depots
• Maintain supply dashboards (eg. month-on-hand) and KPI’s
• Work cross-functionally to ensure supply plans are feasible
• Provide product costs to support international shipments
• Develop and implement appropriate Supply Chain SOPs.

Requirements:

• BS/BA degree in Life Science or a closely related field.
• 6-8 years of experience in a pharmaceutical or biotechnology company
• ASCM CPIM/CSCP certifications preferred
• Working experience with global clinical trials and IRT systems is a must
• Working knowledge of cGMPs and familiarity with US and EU regulations
• Working knowledge of drug development process (Phase I-IV)
• Excellent interpersonal, verbal, and written communication skills are essential in this collaborative, fast-paced, dynamic environment
• Excellent organizational skills and an ability to prioritize effectively to deliver results within established timelines
• Strong attention to detail with excellent follow-up
• Proficient in Microsoft Outlook, Word, Excel, PowerPoint

The pay range that the Company reasonably expects to pay for this headquarters-based position is $165,000 - $185,000; the pay ultimately offered may vary based on legitimate considerations, including geographic location, job-related knowledge, skills, experience, and education.

Applicants must be currently authorized to work in the United States on a full-time basis.

If you are based in California, we encourage you to read this important information for California residents linked here.

Corcept appreciates the commitment and hard work of all our team members as we strive to discover and develop novel treatments for patients with serious unmet medical needs.

 Please visit our website at: https://www.corcept.com/

Corcept is an Equal Opportunity Employer

Corcept 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 Corcept.