Clinical Supply Chain Specialist

Job type:
on-site
Start:
06/2014
Duration:
n.a
From:
Real Staffing
Place:
South San Francisco
Date:
06/03/2014
Country:
flag_no USA
project ID:
715469

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This project is archived and not active any more.
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Essential duties and responsibilities Include but are not limited to the following:


  • The Clinical Supply Chain Coordinator will coordinate with Clinical Operations to assure CTM supply to sites.


  • Responsible for coordinating/tracking bulk shipments and depot-depot shipments.


  • Track and communicate CTM depot level inventories.


  • Initiate and review distribution instructions and protocols.


  • Review and approve reconciliation reports.


  • Work with manufacturing monitors and CMOs to create and review packaging plans, resolve issues and support the packaging activities.


  • Interact as needed with other clinical service providers.


  • Assist Clinical Operations as needed in distribution, handling complaints, returns and destruction of CTM.


  • Other activities as requested.


  • Limited travel.


Requirements:


  • 1-3 years experience in a GXP environment.


  • 2+ years experience in clinical supply management.


  • Proficient in Microsoft Office Platform.


  • Experience in working with CMOs in a virtual environment.


  • Ability to develop timelines and monitor activities required to meet clinical study needs.


  • Working knowledge of clinical cGMPs and regional regulatory requirements for clinical materials and labels.


  • Excellent team skills.


  • Good written and verbal communication skills.


  • Ability to work on a computer for extended periods of time.


  • Regularly required to sit for long periods of time.


  • Regularly required to use hands to operate computer and other office equipment.


Education:


  • Degree in related science or pharmaceutical related field or supply chain management or related experience.