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  • North Chicago, IL 60064

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Project Manager I

KellyMitchell • North Chicago, IL

Posted 2 months ago

Job Snapshot

Other Great Industries
Professional Services, Business Opportunity

Job Description


Project Manager I 

Period: 01/21/2019 to 01/19/2020

Work Location: 1 N Waukegan Road, AP9A, North Chicago, Illinois, 60064-1802


  • Education Requirement: Bachelor’s Degree required preferably in physical science, math, engineering or pharmacy. 
  • Experience: 2+ years total experience in the Pharmaceutical Industry. Preferably experience in one of the following areas: 
  • Drug discovery (eg, Process Chemistry, Analytical Chemistry) 
  • Drug development (eg, Formulation) 
  • Clinical operations (eg, Clinical Project Management) 
  • Supply chain (eg, Clinical Supplies Project Management) 

o    Quality Assurance 

o    Major Responsibilities: 

  • Responsible for the project management of key Clinical Supply Chain activities at the protocol level for pre-clinical and Phase I – II clinical trials 
  • Includes forecasting, planning, scheduling, coordination and execution, ensuring timely availability of investigational drug supplies and related services to clinical sites and depots. 
  • Provides input to Clinical Study Teams to influence clinical protocol design to ensure most efficient utilization of supply chain resources. 
  • Translates clinical study design into packaging design. Authors the study medication and labeling section of the clinical protocol. 
  • Develops protocol specific labeling compliant with applicable global regulations. 
  • Identifies, develops, communicates and tracks project timelines, activities, logistics, and milestones. 
  • Responsible for protocol specific clinical supplies scenario analysis, risk management and contingency planning. Forecasts protocol specific bulk drug product requirements, including comparator agents, ancillary supplies and commodities, including overages. 

o    Critical Success Factors 

  • Understanding of clinical development and global supply chain requirements. 
  • Competent in the application of standard business requirements (for example SOPs, Global Regulations). 
  • Understanding the importance of compliance in a regulated environment and be capable of applying this knowledge to daily work. 
  • Ability to work collaboratively within the dept as well as cross-functionally including interacting in a tactful, professional and effective manner. 
  •  Ability to work effectively and professionally with those in the dept as well as Clinical, QA, Analytical and any area interface. 
  •  Ability to manage and prioritize multiple tasks. 
  • Project Management skills. 
  • Good communication skills (both written and oral).
Job ID: 86523
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