Highlights and Considerations for Transfer of Sponsorship in Clinical Research
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|---|---|---|---|---|
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About this course
Reasons to attend
This course provides Clinical Project Managers (CPMs) with essential knowledge on managing and documenting the transfer of sponsorship in clinical trials. It focuses on ensuring continuous study oversight, maintaining patient safety, and effectively managing stakeholders' new roles and responsibilities.What's included?
- Documents and materials related to this course are included
- Globally recognised certificates awarded after test completion
Course schedule
We provide this course in two distinct formats: Classroom OR Online| 1-Day face-to-face: 09:00 - 17:00 | 2 webinar sessions of 3 hours |
Course Description
In this 1-day training (or two 3-hour webinars), you will gain crucial insights into the complexities of transferring sponsorship in clinical research. This course is specifically designed for you to address the unique challenges in maintaining study continuity and patient safety during sponsorship transitions.You'll explore key aspects of sponsor responsibilities, cultural considerations, and regulatory compliance. Through interactive sessions, you'll develop the "power skills" needed for smooth transitions and effective stakeholder management. The course combines high-level overviews with deep-dive discussions, allowing you to analyse potential risks using real-life scenarios.
Join us to enhance your ability to extract best practices, address unspoken concerns, and en-sure open communication with new partners. By the end of this course, you will be equipped with practical strategies to navigate sponsorship transfers successfully, focusing on continuous study oversight and patient safety.
Programme highlight
- Understanding sponsor responsibilities in clinical research
- Key elements of transferring sponsorship while ensuring GCP compliance
- Cultural points and regulatory considerations in sponsorship transfer
- Essential "power skills" for Clinical Project Managers
- Stakeholder identification and interaction improvement
- Interactive risk analysis using real-life scenarios
- Open Q&A session on risk management in sponsorship transfer.
Learning objectives
- Explain the key responsibilities of sponsors in clinical research
- Identify critical elements for ensuring continuity in clinical trials during sponsorship transfer
- Apply GCP principles in the context of changing sponsorship
- Develop strategies for updating processes while maintaining compliance
- Analyse potential risks associated with sponsorship transfer
- Formulate solutions to address identified risks in sponsorship transitions
- Create effective communication strategies for interacting with new partners
Who should attend
- Clinical Project Managers (CPMs) involved in the transfer of sponsorship in clinical trials
- Professionals with experience in clinical research and a good understanding of GCP
- Individuals seeking to enhance their skills in managing transitions in clinical trial sponsorship
Competencies
Trainers
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