Clinical Project Manager

3 days ago


Slough, Slough, United Kingdom MSI Pharma Full time

Job Summary:

MSI Pharma is seeking a highly skilled Clinical Project Manager to lead Clinical Study Teams across Phase 1 studies. As a key member of our team, you will be responsible for overseeing the planning, execution, and delivery of clinical trials.

Key Responsibilities:

  • Study Planning and Execution: Develop and implement detailed study plans, ensuring timely and seamless access to bioanalytical and/or safety data for review meetings.
  • Team Leadership: Lead and manage cross-functional teams, including CRO/Phase 1 Unit partners, to ensure successful trial execution.
  • Risk Management: Perform risk assessments and develop risk mitigation plans to ensure trial subject safety and data quality.
  • Contract Management: Ensure scope changes are tracked, endorsed, and reflected in contract amendments before implementation of activities by the CRO/Phase 1 Unit.
  • Performance Monitoring: Regularly review CRO/Phase 1 Unit performance using KPIs, metrics, and deliverables to ensure trial subject safety, data quality, and critical activities are on track.

Requirements:

  • Education: Bachelor's degree or equivalent in a scientific or healthcare discipline.
  • Experience: 3+ years of clinical project management experience, including leading and managing cross-functional teams.
  • Knowledge: Working knowledge of GCP/ICH requirements, international regulatory guidelines, and the drug development process.

What We Offer:

As a Clinical Project Manager at MSI Pharma, you will have the opportunity to work on complex clinical trials, develop your leadership skills, and contribute to the success of our company.


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