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Remote Clinical Supply Chain Manager
Contract : North Chicago, Illinois, US
Salary Range : 60.00 - 73.00 | Per Hour
Job Code : 358156
End Date : 2025-02-28
Days Left : 6 days, 2 hours left
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Job Description : Role Overview :
Clinical Supplies Project Management (CSPM) team is seeking a Clinical Project Manager II to oversee clinical supply activities across global clinical trials (Phase I-IV). The role ensures timely and accurate drug supply by managing forecasting, packaging runs, and cross-functional coordination. This is a high-impact position requiring expertise in clinical supply chain management, regulatory compliance, and global trial logistics.
Key Responsibilities :
Oversee long-term packaging runs to ensure drug supply meets patient needs.Develop and maintain drug supply forecasts, dynamically adjusting based on trial timelines.Coordinate supply chain activities for global and regional clinical trials across multiple therapeutic areas.Review and refine the drug supply sections of clinical protocols in collaboration with medical writers.Work with regulatory teams to address study-specific requirements and compliance standards (FDA, EMA, etc.).Ensure adherence to GXP standards and global regulatory guidelines for clinical supply management.Work closely with drug supply managers, labeling teams, quality assurance, logistics, and IRT teams.Coordinate with internal and external stakeholders to align supply chain activities with trial objectives.Utilize forecasting tools and IRT systems to manage and track clinical trial supply needs.Leverage Excel and SharePoint for data management, planning, and procedural updates.Participate in industry-leading CSPM training programs to enhance process knowledge.Identify and implement process improvements to streamline clinical supply management.Qualifications :
Experience & Technical Knowledge
5 years of Clinical Supplies Project Management experience (preferred).Strong background in clinical trial logistics, global regulatory compliance, and drug supply forecasting.Familiarity with global regulatory standards (FDA, EMA, etc.) and import / export logistics.Hands-on experience with IRT systems and forecasting tools (preferred but not mandatory).Proficiency in Excel and SharePoint for supply planning and documentation.Key Skills & Attributes
Proactive problem-solving : Ability to dynamically adjust forecasts and manage potential supply chain risks.Strong cross-functional collaboration : Experience working with internal teams across regulatory, logistics, and quality functions.Global clinical trial expertise : Understanding of international trial regulations and logistical considerations.Minimal onboarding required : Ideal candidates should be seasoned in clinical supplies project management and require minimal industry training.Pay Range : $60 / hr. - $73 / hr.
Job Requirement
Clinical Supply ChainProject ManagementFDA / EMA / GXPClinical Trials (Phase I - IV)Drug suppliesPharmaceuticalExcelReach Out to a Recruiter
RecruiterEmailPhoneVishnu Nairvishnu.nair@collabera.comApply Now
Salary : $60 - $73
