What is the role of a Clinical Research Associate (CRA) and how can a MSL support?
Book a session
Date | Product | Location | Price | |
---|---|---|---|---|
What is the role of a Clinical Research Associate (CRA) and how can a MSL support? | eLearning | USD 105 | Book | |
If you would like to have this course as an in-house session click here |
About this course
Reasons to attend
In this course, we will explore the crucial role of a Clinical Research Associate (CRA) and how a Medical Science Liaison (MSL) can support them.You'll learn the fundamentals of the CRA role and how they work to ensure the safety and efficacy of clinical trials. You'll gain an understanding of who the stakeholders are that a CRA works with and how to constructively work together at an investigational site.You'll also learn how an MSL can support a CRA by providing critical medical and scientific knowledge, and by building relationships with key stakeholders. By working together, the CRA and MSL can help to bring new treatments to patients more quickly and safely.Course Description
Throughout the course, you'll learn about the daily activities of a CRA and an MSL and how they collaborate to ensure the safety and efficacy of clinical trials. You'll understand the monitoring activities and responsibilities of a CRA in relation to Good Clinical Practice (GCP) and regulations.In this course, we'll explore the critical tools and techniques used by CRAs, including site qualification, site initiation, and monitoring visits. You'll learn about the daily activities of an MSL, from providing medical and scientific knowledge to building relationships with key stakeholders.We'll also discuss the collaboration between CRAs and MSLs, exploring the areas where they can meet to ensure that new treatments are brought to patients more quickly and safely. You'll understand the importance of collaboration in clinical research, and how the teamwork between CRAs and MSLs can drive success.Programme highlight
- Role of the CRA: Monitoring activities & responsibilities in relation to GCP and regulations
- Daily activities of a CRA
- Daily activities of an MSL
- Collaboration between CRA and MSL: Where can/do they meet?
Learning objectives
- Understand what a CRA is doing and why
- Know who are the stakeholders a CRA is working with
- Be able to constructively work with CRAs in doing clinical trials at an investigational site
Who should attend
Whether you're just starting out in clinical research or are an experienced professional looking to broaden your knowledge, this course is an essential resource for understanding the critical role of a CRA and how an MSL can support them.
Competencies
This course covers competencies that are part of the ECCRT Competency Framework
- Scientific Concepts & Research Design
- Ethical & Participants Safety Considerations
- Investigational Product Development and Regulation
- Clinical Studies Operations (GCPs or ISO 14155)
- Study and Site Management
- Data Management and Informatics
- Leadership and Professionalism
- Communication
- Teamwork
- Business acumen
No testimonial yet