Course Description
Essentials of Clinical Research
Alison
Learn about core principles, ethical considerations and good clinical practice in this free online training course. Clinical research seeks to evaluate the safety and efficacy of treatments and medications. This course will expose you to the many stakeholders’ roles and obligations and how to ensure compliance with the regulations and guidelines. For precise and reliable data, we use clinical trial design and data management. Investigate clinical trial protocols and ethical concerns to ensure the safety and well-being of participants.
Online Course
| Course Code | 5968 |
| College Name | Alison |
| Course Category | Education, Education Studies, Health Care |
| Course Type | Online Learning |
| Course Qualification | CPD Certificate |
| Course Location | Online Course |
| Delivery mode | |
| Course Fee | Free |
| Course Duration | 1.5-3 hours |
| Entry Requirements | Like all courses on the Alison Free Learning platform this is a free, CPD-accredited course. A Graduate can choose to buy a certificate or diploma upon successful completion of a course, but this is not required or necessary. At Alison we believe that free education, more than anything, has the power to break through boundaries and transform lives. Alison is the world’s largest free online empowerment platform for education and skills training, offering over 5000 CPD accredited courses and a range of impactful career development tools. It is a for-profit social enterprise dedicated to making it possible for anyone, to study anything, anywhere, at any time, for free online, at any subject level. Through our mission, we are a catalyst for positive social change, creating opportunity, prosperity, and equality for everyone. |
| Career Path | In This Free Course, You Will Learn How To • List the different roles and responsibilities in clinical research • Identify the regulatory affairs in clinical research • Explain the concept of clinical data management • Outline the principles of good clinical practice • Describe monitoring and auditing clinical trials • Review the good clinical practice guidelines • Recall the clinical trial reporting requirements • Discuss the basics of biostatistics in clinical research • Indicate the design of clinical trials • State how to design a clinical trial protocol • Discuss the ethical consideration in clinical research |
For information about Alison, please visit our college page on www.nightcourses.com by clicking here.
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