Clinical Project Manager

  • location: North Chicago, IL
  • type: Contract
  • salary: $35 - $38.03 per hour
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job description

Clinical Project Manager

job summary:
  • 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.
 
location: North Chicago, Illinois
job type: Contract
salary: $35.00 - 38.03 per hour
work hours: 9 to 5
education: Bachelors
 
responsibilities:
  • 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.
 
qualifications:
  • 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)
    • Quality Assurance
  • 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).
 
skills: SOP, Clinical Trial Supply Strategy
Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

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