The Opportunity

We're looking for a Project Manager, working in the Pharmaceuticals & Medical Products industry in Redwood City, California, United States.

  • Supports the financial aspects of the projects (i.e., creating and managing budgets, setting up vendor contracts and purchase orders, tracking invoices, and accruals).
  • Supports managing team meetings (agendas, action items, status reports).
  • Supports vendor management.

The pay range we're offering is 100 to 110 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
  • BA/BS degree in a relevant science discipline (higher degree preferred)
  • 5 years of experience in drug development within the pharmaceutical industry
  • CMC design, development and technical support experience from Phase I to late stage development and/or post launch phases
  • In depth knowledge of project management as a discipline including the ability to create, coordinate, and maintain an integrated product plan and to control or respond to changes in strategy and scope
  • Understanding of financial and resource planning systems and processes and ability to coordinate project-level budget/resource estimates and manage actuals vs. plan
  • Preferable inhalation product development, clinical/commercial supply chain, regulatory experience with ideally good knowledge of the broader business especially development, commercialization, post-launch technical support and lifecycle management
  • Demonstrated strong interpersonal and communication skills (credible and persuasive)
  • Proactive, forward-thinking and creative with high ethical standards and a team player with leadership skills and ability to influence others to achieve successful outcomes and meet timelines
  • Familiarity with domestic and international cGMP regulations and industrial guidance documents (CFRs, ICH)
  • Self-motivated and willing to accept responsibilities outside of initial job description
  • Ability to handle multiple project and priorities with exceptional organizational, attention to detail and time management skills
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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