Administration of Clinical Research
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Summary
- Digital certificate - Free
- Reed Courses Certificate of Completion - Free
- Tutor is available to students
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Overview
Understanding the nuances of administration is crucial in the evolving field of clinical research. Enter a world where innovation and accuracy collide, allowing you to see the healthcare of the future right before your eyes. Learn how to easily handle the challenges of ethics, regulatory compliance, and trial design. Discover the secrets to effective data management and reporting, making sure that each stage complies with the strictest quality and integrity requirements. Explore the crucial area of adverse events and safety reporting, where success is largely dependent on alertness. Discover the fine art of clinical trial auditing and monitoring, wherein results and participants are protected by meticulous attention to detail.
Key Features:
- CPD Certified
- Free Certificate from Reed
- CIQ Approved
- Developed by Specialist
- Lifetime Access
CPD
Curriculum
Course media
Description
Welcome to the clinical research of the future, where your knowledge influences the discoveries of the future.
Course Curriculum
- Module 1: Introduction to Clinical Research Administration
- Module 2: Clinical Trial Design and Planning
- Module 3: Ethics and Regulatory Compliance
- Module 4: Institutional Review Boards (IRBs) and Ethics Committees
- Module 5: Data Management and Recordkeeping
- Module 6: Safety Reporting and Adverse Events
- Module 7: Clinical Trial Monitoring and Auditing
- Module 8: Study Site Management and Quality Control
- Module 9: Data Analysis and Reporting
- Module 10: The Future of Clinical Research
Learning Outcomes:
- Master clinical trial design strategies for optimal planning.
- Navigate ethical and regulatory frameworks with confidence and precision.
- Implement robust data management systems for seamless recordkeeping.
- Ensure safety reporting protocols meet industry standards and requirements.
- Conduct thorough clinical trial monitoring and auditing processes effectively.
- Utilise site management techniques to uphold quality control standards impeccably.
Who is this course for?
- Aspiring clinical research administrators seeking comprehensive knowledge.
- Healthcare professionals transitioning into clinical research roles.
- Individuals passionate about contributing to advancements in healthcare.
- Researchers eager to enhance their understanding of trial administration.
- Students pursuing careers in pharmaceuticals or healthcare management.
Career path
- Clinical Research Coordinator
- Regulatory Affairs Specialist
- Data Manager
- Quality Assurance Auditor
- Clinical Trial Monitor
- Research Analyst
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Certificates
Digital certificate
Digital certificate - Included
Reed Courses Certificate of Completion
Digital certificate - Included
Will be downloadable when all lectures have been completed.
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This course is advertised on reed.co.uk by the Course Provider, whose terms and conditions apply. Purchases are made directly from the Course Provider, and as such, content and materials are supplied by the Course Provider directly. Reed is acting as agent and not reseller in relation to this course. Reed's only responsibility is to facilitate your payment for the course. It is your responsibility to review and agree to the Course Provider's terms and conditions and satisfy yourself as to the suitability of the course you intend to purchase. Reed will not have any responsibility for the content of the course and/or associated materials.
