Project Manager III

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The Opportunity

We're looking for a Project Manager III, working in the Pharmaceuticals & Medical Products industry in Meriden, Connecticut, United States.

  • Provides high quality project support to Project Leaders (PL).
  • Develops and creates integrated detailed operational project plans, analyzes and monitors the project timelines, impact of risks, resources and costs (investments) with integrated risk management, reflecting the selected strategy for projects.
  • Analyses the project plan and timelines along the product value chain and ensures optimal critical path.
  • Develops scenarios from project need phase, elaborates first cost/timelines estimate and up to the end of the project provides recommendation for optimization.
  • Ensures the collaboration with all the planners from the project involved platforms or the enabling functions to guarantee consistency between the project plan and the operational plan.

The pay range we're offering is 84 per hour. This position may present an opportunity to go permanent.

Our Client

Our client is an award-winning clinical development company.  Improving lives globally with 20+ years’ experience in clinical research and strategic resourcing.  Elevating results with proven strategies, comprehensive solutions, and customized delivery models.

Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations.

Strong relationships provide you connections and access to great opportunities.  Industry expertise sets you up for success with helpful insights, career coaching, and professional training.  Grow and learn while you put your skills to work.  

Experience Required for Your Success
  • MS, PharmD, Engineer degrees in one of the areas of drug development or production
  • Experience in vaccine development preferred
  • 3-5 years of project management experience within the pharmaceutical industry
  • Excellent analytical skills to understand and transform project activities, deliverables and milestones into a database structure
  • Good Microsoft office packages literacy and ability to understand various computer software and data bases
  • Planisware literacy preferred
  • High willingness and ability to become acquainted with new fields (e.g. Vaccine Development, Industrialization, Launch Readiness)
  • Ability to cooperate transversely with many partners from different part and level of the organization
  • Experience in using databases and Project Management tools (e.g. Planisware, MS Project, Gantt Chart, Excel, etc.)
  • Knowledge of CMC activities and requirements (industrial development and manufacturing)
  • Good knowledge of pharmaceutical regulatory guidelines related to requirements, quality and change control
What Do You Think?

Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible? Apply here.

Not exactly? Join Our Talent Community, and we'll let you know of additional opportunities.


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