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Curricular information is subject to change
On completing this activity, students will be expected to be able to participate effectively in any real life professional learning experience by integrating into a research team and apply their academic experience and their theoretical knowledge in a professional research setting.
Specifically students will:
Understand Good Clinical Practice
Understand Ethics and Consent
Understand clinical trial management (including budgets and costing, project management and risk management)
Understand study start up and monitoring
Understand Regulatory and Quality Systems
This module introduces important concepts in clinical trial management including, ethical, legal and social issues
Student Effort Type | Hours |
---|---|
Lectures | 55 |
Autonomous Student Learning | 160 |
Total | 215 |
Not applicable to this module.
Description | Timing | Component Scale | % of Final Grade | ||
---|---|---|---|---|---|
Assignment: Case study | Varies over the Trimester | n/a | Graded | No | 50 |
Assignment: Protocol Review | Coursework (End of Trimester) | n/a | Graded | No | 50 |
Resit In | Terminal Exam |
---|---|
Autumn | No |
• Feedback individually to students, post-assessment
• Online automated feedback
Students receive feedback throughout the module, following submission of components Students also receive regular feedback through quizzes
Name | Role |
---|---|
Dr Deborah Wallace | Lecturer / Co-Lecturer |