Conducting Remote Monitoring and Risk-Based Monitoring as a CRA

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Description

Masterclass: Conducting Remote Monitoring and Risk-Based Monitoring as a CRA
Are you an aspiring or early-career clinical research professional wanting to enhance your industry skills to enhance your CV and job-readiness? In the dynamic clinical research industry, remote monitoring and risk-based monitoring (RBM) have become essential methodologies for Clinical Research Associates (CRAs) aiming to ensure data integrity and regulatory compliance without having to be physically onsite. This concept of RBM was introduced since ICH-GCP E6 R2.

Our 2-hour interactive masterclass is designed to equip anyone who’s aspiring to become a CRA or early-career CRAs with the knowledge and practical skills necessary to effectively implement these modern monitoring approaches in clinical trials.

🎯 This masterclass is part of our award-winning Industry-Bridging Program (IBPTM), 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 Efficiency: Develop the ability to conduct effective remote monitoring, reducing the need for frequent on-site visits while maintaining data quality.
• Improved Risk Management: Implement RBM strategies to proactively identify and mitigate potential issues in clinical trials.
• Regulatory Adherence: Ensure compliance with current regulatory standards for monitoring, minimizing the risk of non-compliance.
• Professional Development: Expand your skill set with contemporary monitoring techniques, increasing your value in the clinical research field.

By participating in this masterclass, you’ll gain practical insights and tools to excel in conducting remote and risk-based monitoring as a Clinical Research Associate, ensuring the highest standards of data integrity and regulatory compliance in your clinical trials.

What You’ll Learn:

• Foundations of Remote Monitoring: Understand the principles and benefits of remote monitoring, including strategies for data review, query management, and identifying site compliance issues without physical visits.
• Risk-Based Monitoring (RBM) Strategies: Explore the core concepts of RBM, focusing on prioritizing monitoring activities based on risk assessment to enhance efficiency and resource allocation.
• Regulatory Guidelines and Compliance: Gain insights into the regulatory frameworks governing remote and risk-based monitoring, ensuring adherence to Good Clinical Practice (GCP) and other relevant guidelines.
• Data Management and Centralised Monitoring: Learn how to utilize centralized data aggregation and statistical monitoring techniques to oversee trial progress and maintain data quality.
• Practical Application and Case Studies: Engage with real-world scenarios to apply remote and RBM methodologies, enhancing problem-solving skills and decision-making in clinical trial monitoring.

Who Should Attend?

• Aspiring and early-career Clinical Research Associates (CRAs): Professionals seeking to update their monitoring practices with remote and risk-based methodologies.
• Clinical Trial Managers and Coordinators: Individuals responsible for overseeing trial operations who wish to implement efficient monitoring strategies.
• Regulatory Affairs Specialists: Personnel aiming to understand the compliance aspects of modern monitoring approaches.
• Data Managers: Professionals involved in data oversight looking to integrate centralized monitoring techniques.

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.