Masterclass: Performing Source Document Verification (SDV) and Routine On-Site 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? 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.

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?

This masterclass is ideal for:

· 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.

Key Benefits of Attending:

· 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.

📅 Date: 25 May 2025
📍 Format: Live Virtual Masterclass. This online event is held via Zoom. Meeting link other information including templates, and case studies will be delivered via email upon registration and before class.
⏳ Time: 2:30 pm AEST – 4:30 pm AEST
💰 Cost: $150 + GST

📃Certification: Each attendee will receive a certificate of completion to boost your CV and enhance your employability.

🎯 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.

👩‍🎓 IBP trainees: Follow the instructions provided during Program onboarding.

✨ Early Bird Discount: Save 20% when you register before 16 May 2025!
✨ Group Discount: Enrol with 2 or more colleagues and save 30%!

📢 Referral Bonus!

Share this event with your network! For every friend or colleague you refer who registers, you’ll receive an addition 10% discount on your own ticket! Plus, the person you refer will get a 10% special discount too!