Our Clinical Project Management course offers comprehensive training in managing clinical trials from initiation through to closeout. Developed by industry experts with extensive clinical trial and project management experience, this course provides a solid foundation in project management principles, Good Clinical Practice (GCP), and Good Documentation Practices (GDP), essential for ensuring data integrity and regulatory compliance.
Key Learning Outcomes:
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Clinical Trial Lifecycle Management: Gain proficiency in managing clinical trials from study start-up to closeout, including protocol development, site selection, and monitoring.
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Regulatory Compliance: Understand and apply GCP and GDP standards to ensure adherence to regulatory requirements and maintain data integrity.
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Project Planning and Execution: Learn to develop detailed project plans, manage timelines, budgets, and resources, and implement risk management strategies.
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Team Leadership and Communication: Enhance skills in leading cross-functional teams, stakeholder communication, and conflict resolution.
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Documentation and Reporting: Master the creation and maintenance of essential clinical trial documentation, ensuring compliance with regulatory standards.
Who Should Enrol:
This course is ideal for professionals in the pharmaceutical, biotechnology, and clinical research sectors, including:
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Clinical Project Managers
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Clinical Research Associates (CRAs)
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Clinical Trial Assistants (CTAs)
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Regulatory Affairs Specialists
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Quality Assurance and Compliance Officers
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Medical Affairs Professionals
Download Course Summary Leaflet
Click the link above to explore the complete course content in our PDF leaflet.
