Clinical Research Project Manager Checklists
Clinical research project management juggles science, compliance, and logistics simultaneously. This Clinical Research Project Manager Checklists provides the systematic approach that keeps studies on track, in compliance, and within budget. From protocol to publication, manage complexity with confidence.
Project Initiation Checklist
□ Review and understand protocol completely
□ Develop project charter and scope document
□ Create comprehensive project plan
□ Establish project timeline and milestones
□ Define team roles and responsibilities
□ Set up project communication plan
□ Identify and document project risks
□ Establish budget and resource allocation
Site Selection & Activation
□ Identify potential research sites
□ Conduct site feasibility assessments
□ Review site capabilities and resources
□ Evaluate investigator qualifications
□ Conduct site selection visits
□ Complete site contracts and budgets
□ Coordinate site initiation visits
□ Ensure regulatory document collection
Regulatory Management
□ Prepare regulatory submission packages
□ Track IRB/EC submissions and approvals
□ Maintain regulatory binders (TMF)
□ Ensure protocol compliance
□ Manage protocol amendments
□ Coordinate safety reporting
□ Maintain investigator site files
□ Prepare for regulatory inspections
Budget & Financial Management
□ Develop detailed project budget
□ Track study costs and expenses
□ Process site payments
□ Monitor budget variance
□ Manage vendor contracts
□ Review and approve invoices
□ Conduct financial reconciliation
□ Prepare financial reports
Team Management
□ Recruit and onboard team members
□ Conduct team training sessions
□ Define clear roles and expectations
□ Hold regular team meetings
□ Monitor team performance
□ Address conflicts and issues
□ Provide feedback and coaching
□ Manage resource allocation
Vendor Management
□ Identify required vendors (CRO, labs, etc.)
□ Develop vendor selection criteria
□ Conduct vendor assessments
□ Negotiate contracts and budgets
□ Monitor vendor performance
□ Manage vendor relationships
□ Review vendor deliverables
□ Conduct vendor audits
Patient Recruitment & Retention
□ Develop recruitment strategy
□ Create recruitment materials
□ Monitor enrollment progress
□ Implement retention strategies
□ Track screen failures
□ Address recruitment challenges
□ Coordinate with sites on recruitment
□ Report recruitment metrics
Data Management
□ Develop data management plan
□ Design case report forms (CRFs)
□ Set up EDC system
□ Create data validation checks
□ Monitor data quality
□ Manage database lock process
□ Coordinate data cleaning
□ Prepare for database audit
Monitoring & Quality Assurance
□ Develop monitoring plan
□ Schedule monitoring visits
□ Review monitoring reports
□ Track and close action items
□ Manage protocol deviations
□ Oversee CAPA implementation
□ Coordinate quality audits
□ Prepare for inspections
Safety Management
□ Establish safety monitoring plan
□ Set up SAE reporting process
□ Coordinate DSMB meetings
□ Review safety signals
□ Manage safety database
□ Ensure timely safety reporting
□ Communicate safety updates
□ Maintain safety documentation
Communication Management
□ Develop communication matrix
□ Schedule regular status meetings
□ Prepare progress reports
□ Manage stakeholder expectations
□ Coordinate team communications
□ Distribute important updates
□ Maintain communication logs
□ Facilitate issue resolution
Risk Management
□ Conduct risk assessments
□ Develop risk mitigation plans
□ Monitor risk indicators
□ Update risk register regularly
□ Implement contingency plans
□ Report critical risks
□ Review lessons learned
□ Adjust strategies as needed
Study Closure
□ Develop closure plan
□ Coordinate final monitoring visits
□ Ensure data completeness
□ Manage database lock
□ Archive study documents
□ Close out vendor contracts
□ Complete financial reconciliation
□ Prepare final study report
How the Clinical Research Project Manager Checklists works
Define study phase, complexity, and regulatory requirements. Input team structure and site network. The AI generates role-specific clinical research project manager checklists covering all project phases. Include milestone tracking, risk management, and stakeholder communication. Create study-specific adaptations.
Clinical trials fail for preventable reasons: poor planning, missed requirements, and communication failures. This checklist provides the structure that experienced PMs use intuitively. It’s the difference between firefighting and systematic execution.
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