Booking options
£12
£12
On-Demand course
All levels
Take on a transformative journey into the dynamic realm of Clinical Research Administration. Ever felt the frustration of navigating the complex landscape of clinical trials? The intricacies of trial design, ethical considerations, and regulatory compliance can often be overwhelming. Fear not, as our comprehensive course offers a remedy to these challenges.
Picture yourself gaining mastery over the intricacies of data management, ensuring meticulous record-keeping that forms the backbone of successful clinical trials. Delve into the ethical core of research, understanding the nuances of compliance and the vital role of Institutional Review Boards. Experience the power of effective site management and quality control, fostering environments where trials thrive.
As the course unfolds, witness the evolution of clinical research, foreseeing the future trends that shape the landscape. Break free from the frustration of uncertainty, and step confidently into the world of Clinical Research Administration. Let this course be your guide, equipping you with the knowledge and skills to navigate, excel, and shape the future of clinical research. Your journey awaits - embrace the transformation.
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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