$100K — $150K *
Reviews protocols and designs appropriate supply chain strategy for phase 1-4 global studies. Creates and revises Standard Operating Procedures as required. Designs specifications for automated randomization and drug supply management systems. Oversees variety of logistics issues, including but are not limited to supply chain services, inventory control, import-export, shipment of products and third party warehousing. Identifies key stakeholders within CMC and project teams to ensure on time availability of drug supplies. Leads process improvement efforts and may develop specific department plans and procedures.
As a member of the drug development project teams, this position is responsible for providing comprehensive information about clinical supplies and ensuring continuous supply of clinical trial material for all ongoing studies; ensures on time start up of new studies by having supplies available as required. This position is also responsible for managing clinical packaging and distribution contractors.
QUALIFICATIONS AND REQUIRED SKILLS:
Individual should have a bachelor’s degree and a minimum of 9-10 years relevant experience in the pharmaceutical industry or related medical field. Must have in depth knowledge of clinical supplies and pharmaceutical manufacturing. Must work independently under cGMP, cGCP, and SOPs. Communicates effectively and strategically. Adept at solving complex problems in creative and effective ways. Determines methods and procedures on new assignments.
Valid through: 4/19/2021
$200K — $250K
19 days ago