Performing Source Document Verification (SDV) and Routine On-Site Monitoring as a CRA

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Description

Are you an aspiring or early-career clinical research professional wanting to enhance your industry skills to enhance your CV and job-readiness? Are you an aspiring or early-career clinical research professional aiming to enhance your CV and job readiness? Mastering Source Document Verification (SDV) and conducting effective On-Site Monitoring are critical skills for a successful Clinical Research Associate (CRA).

Our 2-hour interactive masterclass is designed to equip you with the industry’s best practices, expert knowledge and practical skills needed to excel as a CRA, ensuring data integrity and regulatory compliance in clinical trials.

🎯 This masterclass is part of our award-winning Industry-Bridging Program (IBP^TM), which bridges the experience gap by equipping you with the essential job skills, industry knowledge, and real-world experience needed to successfully break into the clinical research industry.

Key Benefits

• Enhanced Monitoring Competence: Develop the skills necessary to perform thorough SDV and effective on-site monitoring, ensuring high-quality clinical trial data.
• Improved Regulatory Compliance: Learn to navigate complex regulatory requirements, reducing the risk of non-compliance during clinical trials.
• Career Advancement: Strengthen your CV with specialised training, increasing your competitiveness in the clinical research job market.
• Practical Application: Engage in interactive sessions that provide hands-on experience with real-world scenarios, preparing you for challenges encountered in the field.

By participating in this masterclass, you’ll gain practical insights and tools to excel in Source Document Verification (SDV) and On-Site Monitoring as a Clinical Research Associate (CRA), ensuring the highest standards of data integrity and regulatory compliance in your clinical trials.

What You’ll Learn:

• Fundamentals of Source Document Verification (SDV): Understand the process of comparing case report form data against original source documents to ensure accuracy and completeness.
• Effective On-Site Monitoring Techniques: Learn how to conduct various types of site visits, including qualification, initiation, routine, and close-out visits, to ensure compliance with study protocols and regulatory requirements.
• Regulatory Compliance and Good Clinical Practice (GCP): Gain insights into adhering to GCP guidelines and maintaining ethical standards during clinical trial monitoring.
• Data Integrity and Quality Assurance: Develop skills to ensure the accuracy, consistency, and reliability of clinical trial data through meticulous monitoring practices.

Who Should Attend?

• Aspiring Clinical Research Associates: Individuals seeking to enter the field of clinical research and develop foundational monitoring skills.
• Early-Career CRAs: Professionals aiming to enhance their proficiency in SDV and on-site monitoring to advance their careers.
• Clinical Trial Coordinators and Managers: Personnel involved in overseeing clinical trial operations who wish to deepen their understanding of monitoring processes.
• Quality Assurance Specialists: Individuals responsible for ensuring compliance and data integrity in clinical research settings.

Format, Date and Time

This is a paid online event. Current Clueo Clinical IBP^TM trainees: please follow the instructions provided during your onboarding.

Attendees will receive access link and password before the event.