Content
1 module
Rating
Course length
25 mins
Instructor
Miranda Schramm
Price
$0 - 95 USD
Description
This course covers the initial steps required to identify and begin a clinical trial. You will also learn the fundamentals of protocol feasibility, handling staff and service providers, managing a draft budget and contract, and how to handle IRB submissions.
Objectives
By the end of this course, learners will be able to:
- Understand the primary steps of the study activation process
- Communicate roles and responsibilities for the regulatory and financial startup of a clinical trial
- Define and contextualize what a coverage analysis is in the early stage of a trial
- Understand core financial startup processes and guidelines
Certificate
By completing/passing this course, you will attain the certificate Advarra Completion Certificate
1.
RRT 200 Clinical Trial Regulatory and Financial Startup
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