Course Description
Course Summary
Upcoming Courses
Learning Objectives
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Understand the core responsibilities and daily activities of a Clinical Project Manager (CPM)
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Navigate the full lifecycle of a clinical trial from a project management perspective
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Develop project plans, timelines, and risk mitigation strategies
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Manage cross-functional teams and vendors
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Communicate effectively with sponsors and stakeholders
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Prepare for CPM interviews with confidence and insight
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Optimize resumes and LinkedIn profiles for trial management roles
Who Should Attend
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Clinical research professionals aiming to move into project/trial management roles
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Clinical Trial Assistants (CTAs), Study Coordinators, or CRAs preparing to transition
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International professionals seeking insight into Canadian/US clinical trial practices
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Anyone seeking a comprehensive understanding of trial management responsibilities and expectations
Course Outline
Module 1
Introduction to Clinical Project Management: Role, Skills & Pathways
Module 2
Clinical Trial Lifecycle: Understanding Key Phases and Milestones
Module 3
Planning and Oversight in Trial Execution (Timelines, Budgets, Risks, Teams)
Module 4
Cross-Functional Team Oversight: Vendors, Sites, and Study Teams
Module 5
Risk Management & Quality Oversight in Clinical Trials
Module 6
Study Start-Up & Trial Management Challenges
Module 7
Communication and Stakeholder Management
Module 8
Real-World CPM Scenarios: Problem-Solving and Decision-Making in Action
Module 9
Interview Prep for CPM Roles + Job Strategy
Module 10
LinkedIn, Resume, and Career Tools to Break into Project Management
Interactive Activities
- •Case Study: Managing a delayed site during study start-up
- •Case Study: Vendor oversight and quality issue resolution
- •Discussion: 'What would you do?' scenarios on team conflict or protocol deviation
- •Resume Review: Group walkthrough of a strong trial manager resume
- •Mock Interview Hot Seat: Real CPM interview questions with coaching
