Contract Clinical Project Manager II / Sr. Clinical Project Manager (Homebased)


Category: Project Manager
Job #: 10682
Location: Anywhere U.S.
Job Type: Contract
Rate / Salary Range: Competitive Rate

One of our partners has a need for a Clinical Project manager II or Sr. Project Manager with 100% utilization available. This is a homebased position located anywhere in the U.S.

Job Responsibilities:
  • Effectively and efficiently manage technical, financial, and functional aspects of the project from start-up through close, with focus including but not limited to data management, clinical operations, medical writing, statistics.
  • Assist with responses to and preparation for RFI (Request for Information) and RFP (Request for Proposals)
  • Ensure successful project team communication and mobilization throughout the lifespan of the project
  • Govern all project management aspects of Phase I-IV clinical trials in accordance with all applicable regulatory and legal requirements and ICH guidelines, including but not limited to:
    • Scheduling and leading project meetings
    • Acting as primary point-of-contact for clinical trial Sponsors
    • Coordinating activities across project teams
    • Managing project tasks proactively and preparing status reports
    • Generating sales leads through the development of relationships with clients
  • Assist with Project Management department general operational activities, such as:
    • Developing and/or revising training material, technology enablement, and SOPs
    • Assisting with set-up and ongoing management of project information repositories
    • Working with Business Operations leaders to develop and write proposals
    • Tracking and assisting with the completion of cost estimates.
  • Have experience with and knowledge of Microsoft Office, various database systems, CTMS systems, and Statistical Analysis systems
Job Qualifications:
  • Minimum Bachelors of Science in a life sciences or health related field.
  • For Clinical PM II, minimum 7 years’ experience in the clinical research field, having gained that experience working directly for a Sponsor or CRO.
  • For Sr Clinical PMs, minimum 10 years’ experience in the clinical research field, having gained that experience working directly for a Sponsor or CRO.
  • Ability to travel up to 50% as required.
  • Previous leadership experience with demonstrated experience in clinical operations, data management, monitoring, regulatory affairs, drug supply, etc.
  • Previous experience as a Clinical PM required.

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