Professional Certificate in Clinical Research Management
-- ViewingNowThe Professional Certificate in Clinical Research Management is a comprehensive course designed to equip learners with the essential skills needed to thrive in the rapidly evolving field of clinical research. This program emphasizes the importance of rigorous scientific inquiry, ethical considerations, and regulatory compliance in clinical trials.
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GBP £ 140
GBP £ 202
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Here are the essential units for a Professional Certificate in Clinical Research Management:
• Introduction to Clinical Research Management: This unit will cover the basics of clinical research management, including the clinical research process, regulations, and ethical considerations.
• Clinical Trial Design and Protocol Development: This unit will focus on the development of clinical trial protocols and study designs, including the selection of appropriate endpoints and statistical analysis plans.
• Site Management and Monitoring: This unit will cover the management of clinical trial sites, including site selection, initiation, monitoring, and closeout.
• Data Management and Analysis: This unit will focus on the collection, management, and analysis of clinical trial data, including data validation, quality control, and statistical analysis.
• Regulatory Affairs and Compliance: This unit will cover the regulations and guidelines that govern clinical research, including ICH-GCP, FDA regulations, and EU clinical trial directives.
• Budgeting and Contract Management: This unit will focus on the financial aspects of clinical research, including budget development, contract negotiation, and financial reporting.
• Project Management for Clinical Research: This unit will cover project management principles and tools that are specific to clinical research, including risk management, stakeholder communication, and project closure.
• Quality Management in Clinical Research: This unit will focus on the implementation and maintenance of quality management systems in clinical research, including quality assurance, quality control, and continuous improvement.
• Clinical Research Ethics and Integrity: This unit will cover the ethical and integrity considerations in clinical research, including informed consent, research misconduct, and data integrity.
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