Sr. Manager, Clinical Supply Chain
Company: BIOMARIN
Location: San Rafael
Posted on: April 15, 2025
Job Description:
Who We AreBioMarin is a global biotechnology company that
relentlessly pursues bold science to translate genetic discoveries
into new medicines that advance the future of human health.Since
our founding in 1997, we have applied our scientific expertise in
understanding the underlying causes of genetic conditions to create
transformative medicines, using a number of treatment
modalities.Using our unparalleled expertise in genetics and
molecular biology, we develop medicines for patients with
significant unmet medical need. We enlist the best of the best -
people with the right technical expertise and a relentless drive to
solve real problems - and create an environment that empowers our
teams to pursue bold, innovative science. With this distinctive
approach to drug discovery, we've produced a diverse pipeline of
commercial, clinical and preclinical candidates that have
well-understood biology and provide an opportunity to be
first-to-market or offer a substantial benefit over existing
therapeutic options.About Technical OperationsBioMarin's Technical
Operations group is responsible for creating our drugs for use in
clinical trials and for scaling production of those drugs for the
commercial market. These engineers, technicians, scientists and
support staff build and maintain BioMarin's cutting-edge
manufacturing processes and sites, provide quality assurance and
quality control to ensure we meet regulatory standards, and procure
the needed goods and services to support manufacturing and
coordinating the worldwide movement of our drugs to patients.Job
Title: Senior Manager, Clinical Supply ChainLocation: Hybrid which
is 2-3 days onsite per week in San Rafael CAAbout the Opportunity:
The Senior Manager, Clinical Supply Chain is responsible for
leading and overseeing the clinical supply chain operations to
support clinical studies with appropriate drug product supply. This
role involves strategic planning, execution, and optimization of
supply chain processes to ensure continuous drug supply from First
Patient In (FPI) through completion of clinical trials. The Senior
Manager will serve as the primary supply chain lead for multiple
clinical programs and act as a key liaison between Technical
Operations (TOPS), Clinical Operations, and study
teams.Responsibilities:Strategic Drug Forecasting and Supply
Planning:
- Develop and implement strategic drug forecasts and associated
supply/distribution plans for multiple clinical trials.
- Initiate and oversee required activities and supply execution
processes, maintaining oversight of production, release, and
distribution steps necessary to ensure continuous drug supply.Team
Leadership and Collaboration:
- Lead and mentor clinical supply chain execution teams,
providing guidance and support to ensure successful delivery of
drug supply.
- Collaborate with Clinical, Manufacturing, and Medical project
managers as well as contract providers to create complex study
forecasts and supply project plans.Clinical Supply Chain Execution:
- Oversee clinical supply chain execution teams and actively
support clinical study teams in all matters related to drug supply
to meet portfolio demands for programs progressing toward critical
milestones.Vendor Management:
- Act as liaison with contractors (CMOs), manage supply budgets,
explore opportunities to optimize budget, complete quarterly
business and performance metrics, and negotiate quotes and work
orders for new trials.Regulatory and Quality Compliance:
- Work with Clinical Operations, QA, and Regulatory to develop
kits and label text for multiple countries/regions and provide
support for IND filings as required.
- Assist in establishing and/or optimizing SOPs, protocols, and
procedures for clinical trial material packaging, labeling, and
distribution to ensure compliance with cGxP
requirements.Documentation and Quality Systems:
- Manage development of pharmacy manuals with appropriate
internal subject matter experts.
- Oversee Quality Systems required documentation, including
Deviations, Investigations, CAPAs, Change Controls, Label and
Product Specifications, and others as required.Project Management:
- Develop and apply Project Plans and Schedules that represent
the appropriate level of detail and task independency.
- Ensure timely follow-up to all commitments in a project plan.
Proactively address risk management issues and implement business
continuity plans.Financial Management:
- Prepare supply and cost forecasts as required. Identify cost
reduction opportunities and develop and manage clinical supply
budget.
- Experience with financial management of supply chain activities
including assisting with departmental budgeting and oversight of
external contracts.Regulatory Inspections:
- Serve as subject matter expert on behalf of TOPS for clinical
trial supply during regulatory inspections.
- Ensure appropriate documentation of IP supply activities is
provided to clinical trial teams for Trial Master File.Additional
Requirements for Senior Role:Leadership and Strategic Vision:
- Demonstrated ability to lead and inspire teams, fostering a
culture of collaboration and excellence.
- Proven track record of developing and executing strategic plans
that align with organizational goals and drive clinical supply
chain success.Advanced Problem-Solving and Decision-Making:
- Strong analytical skills with the ability to identify and
resolve complex supply chain issues.
- Experience in making high-impact decisions that enhance supply
chain efficiency and effectiveness.Extensive Industry Experience:
- Minimum of 7 years of experience in a Clinical Supply Chain /
Contract Manufacturing operation in the pharmaceutical or biotech
industry.
- In-depth knowledge of global Health Authority requirements and
industry best practices.Exceptional Interpersonal Skills:
- Strong interpersonal skills and awareness of the Emotional
Quotient in a corporate environment to interact and resolve
conflicts with many levels inside and outside of the Supply Chain
Logistics organization internationally.Innovative and
Forward-Thinking:
- Ability to drive innovation and continuous improvement within
the clinical supply chain function.
- Experience in implementing new technologies and methodologies
to optimize supply chain processes.Educational Qualifications:
- Advanced degree in Supply Chain Management, Business
Administration, or a related field preferred.This job description
outlines the key responsibilities and additional requirements for a
Senior Manager of Clinical Supply Chain, emphasizing the
leadership, strategic vision, and advanced problem-solving skills
needed for this senior role.Note: This description is not intended
to be all-inclusive, or a limitation of the duties of the position.
It is intended to describe the general nature of the job that may
include other duties as assumed or assigned.Equal Opportunity
Employer/Veterans/DisabledAn Equal Opportunity Employer. All
qualified applicants will receive consideration for employment
without regard to race, color, religion, sex, sexual orientation,
gender identity, national origin, or protected veteran status and
will not be discriminated against on the basis of disability.The
salary range for this position is: $134,400 to $201,600. BioMarin
considers a variety of factors when determining base compensation,
including experience, qualifications, and geographic location.
These considerations mean actual compensation will vary. This
position may also be eligible for a discretionary annual bonus,
discretionary stock-based long-term incentives (eligibility may
vary based on role), paid time off, and a benefits package.
Benefits include company-sponsored medical, dental, vision, and
life insurance plans.For additional benefits information, visit: .
- Eligible employees may participate in benefit plans, subject to
the terms and conditions of the applicable plans.
#J-18808-Ljbffr
Keywords: BIOMARIN, Sacramento , Sr. Manager, Clinical Supply Chain, Professions , San Rafael, California
Didn't find what you're looking for? Search again!
Loading more jobs...