Remote Director, Clinical Supplies
455 Mission Bay Boulevard South San Francisco, CA 94158 US
Job Description
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- Oversee clinical supply activities, encompassing label generation and approval, packaging and labeling operations, release and distribution, expiry extension, cold chain management, and inventory management.
- Facilitate timely startup of new studies through prompt supply availability.
- Manage the Clinical Supply program for investigation drug product inventory management and distribution in partnership with CMOs; evaluates drug utilization versus forecast considering country requirements and logistical timelines.
- Responsible for the oversight of Clinical Supply CMOs.
- Responsible for the management of global strategies in IRT systems.
- Responsible for the creation, periodic review, and maintenance of all Clinical Supply SOPs.
- Accountable for initiating, overseeing, and resolving departmental deviations.
- Collaborate with cross-functional teams (Clinical Operations, QA, CMC, and Regulatory) to ensure optimal execution of Clinical Supply strategy and identify and address potential risks to the progression of clinical programs proactively.
- Function as the internal point person for addressing product issues, temperature excursions, and deviations originating from clinical sites or depots. Collaborate with Quality Assurance to address any quality-related matters.
- Serves as the primary representative/subject matter expert (SME) during all inspections and clinical supply chain audits.
- Serve as a subject matter expert and devise continuous improvement plans for clinical supply GMP, GDP, and business processes.
- Assist in ongoing drug accountability and reconcile end-of-study drug inventory.
- Provide clinical supply and risk mitigation recommendations.
- Oversee inventory management of study drug and comparators at depots.
- Mentor CSC team members as needed on programs and systems.
- B.S. in a scientific, healthcare, or related field with 10+ years of global clinical supply chain experience within the biotechnology sector. APICS certification is advantageous.
- Proven history of establishing, refining, and managing clinical supply chains within the biotechnology industry.
- Solid understanding of GMPs, GCPs, GDPs (GxP) requirements
- Strong attention to detail with excellent follow-up.
- Progressive knowledge of Import/export regulations, including pro-forma invoice generation, import regulations, and global trade compliance.
- Previous successful collaboration & management of third-party CRO’s and CMO clinical supply operations.
- Strong experience of GxP & Systems including development of specifications, oversight of system operations, troubleshooting & identifying gaps, performing set-up & testing of systems, & understanding areas of limitations, risks, or gaps to mitigate. (IRT).
- Exceptional written and verbal communication, with diligence, collaboration, ability to manage complex challenges, and influencing skills.
- Excellent planning, organizational skills, and the ability to work simultaneously on multiple projects with tight timelines.
- Experienced in assisting, as the Clinical Supply Chain SME, during Regulatory Inspections and Audits.
- Proactive in driving performance cross-functionally and fostering collaboration.
- Ability to build/drive internal team consensus.
- Translates broad strategies into specific objectives and action plans.
- Proficient knowledge of MS Office (Smartsheet, Excel, PowerPoint, Visio, Project, etc.)Â
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