Booking options
£24.99
£24.99
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On-Demand course
1 hour 56 minutes
All levels
Explore the intricacies of clinical research and understand the administration process with our Clinical Research Administration Training course. This course will help you deepen your knowledge and acquire the ability to seek career prospects in the relevant sectors.
The course is packed with high;y valuable information on clinical research. From the informative modules, you will learn the core concepts of clinic trial designing and planning. The course will help you develop the skills for data management and analysis. You will be able to build your expertise in monitoring and auditing. Moreover, you will acquire the skills required for quality control and site management as well.
After the course, you will receive a CPDQS-accredated certificate of achievement. This certificate will enhance your employability and help you reach your career goals. Enrol now!
Whether you're an existing practitioner or an aspiring professional, this course is an ideal training opportunity. It will elevate your expertise and boost your CV with key skills and a recognised qualification attesting to your knowledge.
This Clinical Research Administration Training course is available to all learners of all academic backgrounds. But learners should be aged 16 or over to undertake the qualification. And a good understanding of the English language, numeracy, and ICT will be helpful.
After completing this course successfully, you will be able to obtain an Accredited Certificate of Achievement. Certificates & Transcripts can be obtained either in Hardcopy at £14.99 or in PDF format at £11.99.
This exclusive Clinical Research Administration Training course will equip you with effective skills and abilities and help you explore career paths such as
Module 01: Introduction to Clinical Research Administration | |||
Introduction to Clinical Research Administration | 00:15:00 | ||
Module 02: Clinical Trial Design and Planning | |||
Clinical Trial Design and Planning | 00:11:00 | ||
Module 03: Ethics and Regulatory Compliance | |||
Ethics and Regulatory Compliance | 00:13:00 | ||
Module 04: Institutional Review Boards (IRBs) and Ethics Committees | |||
Institutional Review Boards (IRBs) and Ethics Committees | 00:10:00 | ||
Module 05: Data Management and Recordkeeping | |||
Data Management and Recordkeeping | 00:12:00 | ||
Module 06: Safety Reporting and Adverse Events | |||
Safety Reporting and Adverse Events | 00:10:00 | ||
Module 07: Clinical Trial Monitoring and Auditing | |||
Clinical Trial Monitoring and Auditing | 00:09:00 | ||
Module 08: Study Site Management and Quality Control | |||
Study Site Management and Quality Control | 00:17:00 | ||
Module 09: Data Analysis and Reporting | |||
Data Analysis and Reporting | 00:09:00 | ||
Module 10: The Future of Clinical Research | |||
The Future of Clinical Research | 00:10:00 | ||
Certificate and Transcript | |||
Order Your Certificates and Transcripts | 00:00:00 |