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

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.

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.

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.

📍 This live 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.

📃Certification: Each attendee who attends the session will receive a certificate of completion.

🎯 This masterclass is part of our award-winning Industry-Bridging Program (IBP), 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: Please use the discount code provided for registration.

✨ Group Discount: Enrol with 3 or more colleagues and save 30% on the total cost!