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Feedback on this module
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100% of people completing this module said they would recommend it to their colleagues
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100% gave an overall assessment of this module of 7/10 or better
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100% said that this module met their expectations to a level of 7/10 or better
Overview
This module allows the learner to gain an insight into the practical requirements of the Clinical Research Associate (CRA) in the conduct of clinical trials and provides an introduction to drug development. It will check that the user has the required attributes and skills to be a CRA. If you fulfil the criteria the module will review the practical requirements with a view to gaining that first elusive job as a CRA.
The module provides an overview of the role, details the regulatory requirements of a CRA, the ICH GCP responsibilities and gives an insight into how to fulfil these responsibilities. The different types of monitoring visit and the main activities of the CRA when conducting these visits will also be examined.
The module will detail other roles in clinical research that may lead to that of a CRA and also look at the career progression for a Monitor.
The programme is clear and simple in design and gives full instructions for use.
Learning objectives
By the end of this course, you will be able to…
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Describe the role and responsibilities of a clinical research associate / Monitor
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Demonstrate an awareness of the different types of monitoring visit and their objectives
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Outline other roles that may lead to that of a CRA and the possible career opportunities
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Acquire knowledge of the drug industry environment and drug development
Certification & CPD
At the end of the course you can complete a 20 question,
multiple choice exam, which will test you on the subject matter of the
module. The pass mark for the exam is 75%, but you can take the exam as
many times as you like.
On passing the exam you will have the option of printing
out a certificate which will certify your successful completion of the
course.
