Olema Oncology

Associate Director, Clinical Supply Chain

Olema Oncology$185K — $200K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree required; Master's preferred.
  • 10+ years in biotechnology/pharmaceutical clinical supply chain management.
  • Thorough knowledge of Good Manufacturing Practices (GMP).
  • Extensive experience managing forecast demands.
  • Strong global shipping and customs experience.

Responsibilities

  • Plan and optimize end-to-end clinical supply chain management.
  • Implement global Clinical Supply Chain strategies.
  • Manage global inventories and partner with third-party manufacturers.
  • Oversee packaging, labeling, and distribution activities at vendors.
  • Identify supply chain risks and resolve them as needed.

Benefits

  • Competitive compensation package including equity and bonus.
  • Open, flexible, and friendly work environment.
  • Opportunities for long-term career development.
Full Job Description
About the Role >>> Associate Director, Clinical Supply Chain

As the Associate Director of Clinical Supply Chain reporting to the Vice President, 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:
  • 8+ 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.

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About Olema Oncology

Olema Oncology is a clinical-stage biopharmaceutical company that develops targeted therapies for women's cancers. The company's lead product candidate, OP-1250, is a small molecule inhibitor of the estrogen receptor (ER) that is being developed for the treatment of breast cancer. OP-1250 has demonstrated preclinical activity in ER-positive breast cancer models and is currently being evaluated in a Phase 1/2 clinical trial. Olema Oncology is also developing a pipeline of other small molecule inhibitors of the ER and other targets for the treatment of breast and gynecologic cancers.
Learn more about Olema Oncology
Size
50 employees
Industry
Founded
2013
NASDAQ

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