Job Overview:

• Manage all aspects of logistics related to Clinical and Ancillary Supplies services.
• Promote these services to both internal and external clients.
• Responsible for the management of project activities related to clinical and ancillary supplies
• Independently lead the delivery of Clinical and Ancillary supplies component of assigned studies for a large complex global study.
• Responsible for line management of personnel: hiring, mentoring, performance management; ensuring understanding of project specific and department policies and procedures for direct reports in single or multiple offices
• Provide regional supervision of staff concerned with clinical and ancillary supplies start up activities and related project feasibility
• Supervise staff in performance of their day-to-day work, including management of resource allocations
• Work with staff in Project Management, Clinical Trial Design & Strategy, Vendor Management, Regulatory Affairs, Quality Assurance, Business Development and Operations, to provide relevant clinical and ancillary supply data critical to the ability of the organization to develop plans for the successful implementation and conduct of global clinical trials.
• Assure that pre-study, drug supply and labeling processes comply with applicable guidelines and regulations and fulfill client and Fortrea requirements.
• Provide logistical support for clinical and ancillary supply coordination
• Provide input into business development activities
• Act as a subject matter expert (SME) in client focused clinical and ancillary supply workstreams

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Please refer the Job description for details