Booking options
£12
£12
On-Demand course
1 hour
All levels
If you're looking to break into the world of clinical research, the Clinical Research Administration Fundamentals Course offers a straightforward and in-depth introduction to the field. This course will equip you with the essential knowledge and skills needed to navigate the administrative aspects of clinical research. From understanding the different stages of clinical trials to managing documentation and compliance requirements, you'll gain the expertise to support research teams efficiently. Whether you're new to the industry or seeking to build on existing knowledge, this course is designed to make complex topics clear and accessible.
With the rapid growth of clinical research and its pivotal role in medical advancements, the need for skilled professionals is ever-present. This course will guide you through the fundamental principles, including ethics, safety protocols, and regulatory considerations. You'll learn how to manage research documentation, assist with trial set-ups, and support clinical study teams with precision. Plus, with the option to study remotely, you can complete the course at your own pace, making it ideal for those balancing work or other commitments. Get ready to enhance your understanding of this critical industry sector and open the door to career opportunities within clinical research.
Key Features
CPD Accredited
FREE PDF + Hardcopy certificate
Fully online, interactive course
Self-paced learning and laptop, tablet and smartphone-friendly
24/7 Learning Assistance
Discounts on bulk purchases
Course Curriculum
Module 01: Introduction to Clinical Research Administration
Module 02: Clinical Trial Design and Planning
Module 03: Ethics and Regulatory Compliance
Module 04: Institutional Review Boards (IRBs) and Ethics Committees
Module 05: Data Management and Recordkeeping
Module 06: Safety Reporting and Adverse Events
Module 07: Clinical Trial Monitoring and Auditing
Module 08: Study Site Management and Quality Control
Module 09: Data Analysis and Reporting
Module 10: The Future of Clinical Research
Learning Outcomes:
Understand key principles in clinical trial planning and design.
Demonstrate proficiency in navigating ethical and regulatory frameworks.
Develop expertise in data management and rigorous recordkeeping.
Implement safety reporting protocols and manage adverse events effectively.
Conduct thorough clinical trial monitoring and auditing procedures.
Acquire skills in study site management, quality control, and data analysis.
Accreditation
This course is CPD Quality Standards (CPD QS) accredited, providing you with up-to-date skills and knowledge and helping you to become more competent and effective in your chosen field.
Certificate
After completing this course, you will get a FREE Digital Certificate from Training Express.
10 CPD hours / points Accredited by CPD Quality Standards
Individuals aspiring to enter the field of clinical research.
Healthcare professionals seeking to broaden their skill set.
Graduates in life sciences or related disciplines.
Research assistants and coordinators aiming for career advancement.
Regulatory affairs professionals looking to specialise.
Quality assurance personnel in healthcare and pharmaceutical sectors.
Professionals transitioning to roles in clinical trial management.
Anyone keen on staying ahead in the evolving landscape of clinical research.
Clinical Research Coordinator
Regulatory Affairs Specialist
Clinical Data Manager
Quality Assurance Auditor
Clinical Research Associate
Pharmacovigilance Officer
Digital certificate
Digital certificate - Included
Once you've successfully completed your course, you will immediately be sent a FREE digital certificate.
Hard copy certificate
Hard copy certificate - Included
Also, you can have your FREE printed certificate delivered by post (shipping cost £3.99 in the UK).
For all international addresses outside of the United Kingdom, the delivery fee for a hardcopy certificate will be only £10.
Our certifications have no expiry dates, although we do recommend that you renew them every 12 months.
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