Sr. Clinical Supply Chain Contractor (6-Month Contract)
South San Francisco, CA (3 days onsite)
Overview
Our client is seeking an experienced Clinical Supply Chain professional to help ensure uninterrupted supply across ongoing and upcoming clinical trials.
Our client is seeking an experienced Clinical Supply Chain professional to help ensure uninterrupted supply across ongoing and upcoming clinical trials.
This is a highly visible role where you will take ownership of end-to-end clinical supply activities for one or more study programs, working cross-functionally and with external vendors to ensure seamless execution, delivering on-time, compliant, and uninterrupted supply while proactively identifying and mitigating risks.
Key Responsibilities
Own end-to-end clinical supply chain activities for assigned study program(s), including full ownership of supply strategy and execution, potentially including investigator sponsored studies
Translate clinical protocols into demand forecasts and supply strategies
Develop and oversee packaging, labeling, distribution, and return plans
Partner cross-functionally with:
CMC, manufacturing, clinical operations, and external vendors
Drive alignment, decision-making, and execution across stakeholders
Manage external CDMOs in an outsourced model to ensure:
Timely execution of supply plans
Adherence to quality, compliance, and study timelines
Oversee drug supply performance for clinical trials
Monitor inventory and supply forecasts
Conduct ongoing reviews and proactively address risks (e.g., stockouts, delays)
Support monthly supply reviews and long-range planning
Balance program-level strategic planning (3-5 year horizon) with day-to-day study execution
Operate in a GxP-compliant environment, ensuring:
Inspection readiness
Clear documentation and communication
Quickly ramp in a GxP environment, gaining study-level understanding and identifying near-term risks
Identify opportunities to improve processes, workflows, and scalability
Contribute to future-state planning, including automation and planning tools implementation
Operate as a service-oriented function, ensuring uninterrupted drug supply and preventing patient-level stockouts
Maintain compliance as the top priority across all supply activities
Operate effectively in a growing environment with evolving systems and processes
Proactively gather information and drive work forward without defined structure
Build relationships and influence cross-functional teams to drive alignment and decision-making
Required Qualifications
8+ years of experience in clinical supply chain or related clinical operations functions (majority in clinical supply chain)
Strong experience supporting clinical trials on the sponsor side (required)
Proven ability to manage end-to-end clinical supply activities
Experience working with external vendors in an outsourced model
Hands-on experience with IRT systems (platform-agnostic)
Strong analytical skills with proficiency in:
Excel (forecasting, pivot tables, formulas)
Bachelor's degree required
Job Type & Location
This is a Contract position based out of South San Francisco, CA.
Pay and Benefits
The pay range for this position is $65.00 - $85.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
Workplace Type
This is a hybrid position in South San Francisco,CA.
Application Deadline
This position is anticipated to close on Jun 5, 2026.
About Actalent
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