Making Informed CRO Selection for Clinical Trial Success
Book a session
Date | Product | Location | Price | |
---|---|---|---|---|
10/10/2025 | Making Informed CRO Selection for Clinical Trial Success | Brussels | EUR 950 | Book |
If you would like to have this course as an in-house session click here |
About this course
Reasons to attend
Contract Research Organisations (CROs) play a critical role in the success of clinical trials, impacting timelines, data quality, and overall study outcomes. In this comprehensive training program, we equip you with the knowledge and tools necessary to make informed decisions when selecting the most suitable CRO for your clinical research projects.What's included?
- Documents and materials related to this course are included
- Globally recognised certificates awarded after test completion
- This course has been granted PharmaTrain Recognition
Course schedule
We provide this course in two distinct formats: Classroom OR OnlineClassroom: 1-Day face-to-face: 09:00 - 17:00 | Online: 2 webinar sessions of 3.5 hours |
Our specialised course on CRO Selection is designed to provide you with the knowledge and skills needed to navigate the process of selecting the most suitable CRO for your specific trial needs.
The course kicks off by understanding the current CRO market trends and related CRO outsourcing models. Thereafter, you will gain valuable insights into striking the right balance between providing comprehensive trial specifications and avoiding information overload in the Request for Proposal (RFP) to the pre-selected CROs. Finally, the course provides you with the necessary expertise to elicit competitive proposals from potential CRO partners, setting the stage for successful proposal evaluation and comparison.Through hands-on exercises and interactive discussions, you will develop the art of impartial proposal evaluation. By analysing capabilities, costs, timelines, and potential risks, you will fine-tune your decision-making skills, ensuring alignment with trial objectives and timelines.Programme highlight
- Understanding the CRO landscape
- Define the right outsourcing strategy for your organisation
- Define your parameters for a good RFP
- Qualify the right CRO for your project
Learning objectives
- Gain insights on important aspects of how to select the right resourcing strategy
- Learn how to prepare a meaningful RFP
- Get hands-on information on how to qualify the right CRO
- Know how to plan study specific requirements to optimize your project results
Who should attend
Clinical Research professionals responsible for selecting Contract Research Organisations (Project Managers, Clinical Operations Managers, Outsourcing Managers), and anyone working with external providers who has an interest.
Competencies
This course covers competencies that are part of the ECCRT Competency Framework
- Scientific Concepts & Research Design (0)
- Ethical & Participants Safety Considerations (0)
- Investigational Product Development and Regulation (0)
- Clinical Studies Operations (GCPs or ISO 14155) (3)
- Study and Site Management (6)
- Data Management and Informatics (1)
- Leadership and Professionalism (3)
- Communication (3)
- Teamwork (2)
- Business acumen (1)
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