How does the Clinical Trials course help in transitioning into roles like Medical Writing, Data Management, or Regulatory Affairs?
Asked by Jaya Shukla
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1 Answer
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The Clinical Trials course will provide students with a multi-disciplinary basis in trial design, data management, and regulatory requirements. These are transferable skills that can be used in other positions like medical writing, clinical data management, or regulatory affairs.
The general understanding of documentation, data flows, and ethical considerations when conducting research will allow graduates to transfer skills to related areas within the clinical research industry, thereby demonstrating a lot of flexibility for development.
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