Course Overview
Effective patient recruitment and retention are critical to the success of clinical trials. Insufficient recruitment can lead to significant financial losses, while high dropout rates undermine trial integrity, causing delays and incomplete studies. Mastering evidence-based strategies enables clinical research professionals to complete trials on schedule, stay within budget, and achieve reliable outcomes that drive medical advancements.
The Patient Recruitment and Retention in Clinical Trials course equips clinical research professionals with the tools, strategies, and insights to optimize recruitment and retention efforts. Participants will learn to develop patient-centric approaches that boost engagement, reduce dropout rates, and ensure trials achieve their enrolment goals and run smoothly.
Key Learning Objectives
- Understand the importance of patient recruitment and retention in the successful conduct of clinical trials.
- Identify common challenges and barriers to patient recruitment and retention in clinical research studies.
- Learn effective strategies for identifying and engaging eligible participants for clinical trials.
- Explore innovative approaches and technologies for improving patient recruitment and retention rates.
- Understand the ethical considerations and regulatory requirements associated with patient recruitment and retention activities.
- Develop skills in screening, enrolling, and retaining participants in clinical trials while ensuring compliance with study protocols.
- Learn how to tailor recruitment and retention strategies to target specific patient populations and address diversity and inclusion.
- Gain insights into patient-centred approaches to enhance engagement, communication, and support throughout the trial.
- Understand the importance of data monitoring and evaluation in assessing the effectiveness of recruitment and retention strategies.
- Explore best practices for successful patient recruitment and retention efforts in clinical trials.
Course Structure
This course is designed for busy professionals and is delivered through online, self-paced learning with recorded simulations that provide real-life scenarios for effective learning. The course includes:
- Interactive modules covering recruitment and retention fundamentals and strategies.
- Recorded simulations and real-world case studies to apply your learning to practical scenarios, with role-play scenarios for patient engagement.
- Quizzes and assignments to help reinforce your understanding and ensure retention of critical information.
- Final assessment to evaluate your knowledge and award certification upon successful completion.
- Downloadable Resources: Templates, checklists, and guides for effective site monitoring.
- Mode: 100% Online, Self-Paced
- Duration: Approximately 15 hours.
Who Should Enrol?
This course is ideal for:
- Clinical Research Associates (CRAs)
- Clinical Trial Managers
- Clinical Trial Assistants (CTAs)
- Site Coordinators
- Patient Engagement Specialists
- Regulatory Affairs Professionals
Prerequisite
- A bachelor’s degree or equivalent qualification in a relevant field (e.g., Life Sciences, Nursing, or related disciplines).
- Familiarity with basic clinical trial processes and terminology is recommended, but not mandatory.
Certification Requirements
- A minimum score of 80% on the final assessment is required to receive the accredited certification. This certification is a mark of your proficiency in clinical trial regulatory and ethical compliance, recognised by industry leaders.
- Learners have two attempts to pass the assessment. If additional attempts are needed, a fee will apply.
Course Fee
- Cost: $450 AUD inc. GST (12-month access to materials and resources)
- Discounts: Available for group enrolments and members (10%-30% off)
- For all inquiries, please contact info@citium.academy