BeiGene, Ltd.

Clinical Supply Chain Specialist

BeiGene, Ltd.$79K — $109K *
US-AnywhereRemote in United States
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's or Master's degree in Business Administration, Operations Management, or related field.
  • Minimum of 7 years in supply chain experience, preferably in biotech, pharmaceutical, or CRO industries.
  • Strong knowledge of clinical supply best practices and IRT systems.
  • Experience working in a cGMP environment.
  • Proficient in developing and implementing supply plans and processes.

Responsibilities

  • Represent Clinical Supply Chain in Clinical Study Teams and collaborate with internal stakeholders.
  • Align clinical demand requirements with supply plans and timelines.
  • Create and manage supply and inventory plans for clinical trial materials.
  • Oversee adherence to production schedules and make necessary corrections.
  • Manage GMP inventory, including reporting and drug accountability.
  • Oversee relationships with CMOs and distribution vendors to ensure efficient operations.
  • Lead investigations into exceptions and drive root cause analysis solutions.

Benefits

  • Comprehensive benefits package including Medical, Dental, and Vision coverage.
  • 401(k) with company matching contributions.
  • Flexible spending accounts (FSA/HSA) available.
  • Paid Time Off (PTO) for work-life balance.
  • Life Insurance coverage for employee protection.
  • Wellness programs to support employee health and well-being.
  • Employee Stock Purchase Plan allowing participation in company equity.
Full Job Description
General Description:

Under the supervision of the direct manager or team lead, the Specialist of Clinical Supply Chain manages drug supply activities related to planning, label development, label & pack, and distribution for clinical trials. With the guidance of the manager or team lead, actively develops and oversees supply plans to ensure accurate and continuous supply to patients while reducing risk and minimizing waste. With guidance, may participates on teams to develop and implement process improvements to build the organization for the future.

Essential Functions of the Job:
  • Work with team lead or manager to understand clinical demand requirements and ensure alignment with study teams to supply plans and timelines.
  • Collaborate and liaise with internal (e.g. Clinical Operations, Regulatory, Quality, CMC) and external stakeholders (e.g. CMOs, IRT vendors) appropriately.
  • With guidance, outline supply strategies to maximize supply efficiency, minimize waste while identifying risk and develop risk mitigation plans.
  • Work with team lead or manager to create supply and inventory plans and develop production schedules for clinical trial materials.
  • Monitor schedule adherence of production schedules and make course corrections if needed.
  • Work with label management team to ensure label text and proofs are in accordance with applicable rules, regulations, product specifications, and clinical study protocol(s).
  • Assist with comparator sourcing team to conduct developed comparator sourcing strategies/activities.
  • Support IRT user acceptance testing, develop IRT supply strategy (DNX parameters), and oversee ongoing supply activities in system.
  • Coordinate and track bulk shipments to CMOs, depots, and vendors. Maintain and track import licenses.
  • Participate in performing UAT acceptance testing for IRT systems
  • Supports IRT related activities to ensure adequate supply for clinical trials
  • Additional responsibilities as required


Supervisory Responsibilities:
  • N/A

Computer Skills:
  • Proficient in Microsoft Word, Excel, and Outlook


Other Qualifications:
  • Good analytical, communication and interpersonal skills.
  • Good organizational and effective time management skills.
  • Good problem-solving and risk management skills.
  • Good at Microsoft Office Tools


Education Required:
  • Bachelor's degree or above in Medicine/science related, or supply chain/management/operation related, or equivalent combination of education, training and experience.
  • 2+ years progressive experience in Supply Chain preferably within the biotech, pharmaceutical, CRO, industry.


Global Competencies

When we exhibit our values of Patients First, Driving Excellence, Bold Ingenuity and Collaborative Spirit, through our twelve global competencies below, we help get more affordable medicines to more patients around the world.
  • Fosters Teamwork
  • Provides and Solicits Honest and Actionable Feedback
  • Self-Awareness
  • Acts Inclusively
  • Demonstrates Initiative
  • Entrepreneurial Mindset
  • Continuous Learning
  • Embraces Change
  • Results-Oriented
  • Analytical Thinking/Data Analysis
  • Financial Excellence
  • Communicates with Clarity


Salary Range: $79,100.00 - $109,100.00 annually
BeOne is committed to fair and equitable compensation practices. Actual compensation packages are determined by several factors that are unique to each candidate, including but not limited to job-related skills, depth of experience, certifications, relevant education or training, and specific work location. Packages may vary by location due to differences in the cost of labor. The recruiter can share more about the specific salary range for a preferred location during the hiring process. Please note that the listed range reflects the base salary or hourly range only. Non-Commercial roles are eligible to participate in the annual bonus plan, and Commercial roles are eligible to participate in an incentive compensation plan. All Company employees have the opportunity to own shares of BeOne Medicines Ltd. stock because all employees are eligible for discretionary equity awards and to voluntarily participate in the Employee Stock Purchase Plan. The Company has a comprehensive benefits package that includes Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness.

About BeiGene, Ltd.

BeiGene, Ltd. is a biotechnology company that develops and commercializes innovative cancer treatments. The company was founded in 2010 and is headquartered in George Town, Grand Cayman. BeiGene's portfolio includes several drug candidates that target cancer cells and the tumor microenvironment. The company's lead product, Brukinsa, is a treatment for mantle cell lymphoma that has been approved by the U.S. Food and Drug Administration (FDA) and the European Medicines Agency (EMA). BeiGene also has partnerships with several pharmaceutical companies, including Amgen, Merck, and Novartis.
Learn more about BeiGene, Ltd.
Size
8,300 employees
Market Cap
$22.2 billion
Industry
Net Income
-$1.5 billion
Founded
2010
5 Year Trend
+305.7%
Revenue
$308.8 million
NASDAQ

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