The Basics

Next Workshop: March 16-17, 2012 Atlanta GA
This workshop brings to life FDA and ICH guidelines for conducting clinical trials by covering a trial from the site perspective in sequence, from pre-study visit to study closeout. The course is designed for new study coordinators (CRCs), research nurses or clinical trial investigators and for any site professional without formal GCP training.

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Beyond the Basics

Next Workshop: March 19-20, 2012 Atlanta GA

This workshop covers clinical trial management  beyond routine coordinating. Topics include basic clinical trial budgeting, medical device regulations, clinical trial protocol analysis, FDA audits, ethical issues and site team communications. This class is targeted at experienced study coordinators (CRCs), research nurses, clinical trial investigators and clinical research site professionals who have attended basic training in clinical trial coordination and/or who have equivalent knowledge of FDA guidelines and GCPs.

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Managing Finances

Next Workshop:  March 5-6, 2012 San Francisco CA

This workshop covers clinical trial finances from using financial protocol analysis to build a trial budget to tracking financial activity and working with financial reports. This class is for experienced clinical research nurses, study coordinators (CRCs), investigators, research administrators or any clinical team member with a fiscal responsibility. Attendees should have attended basic training in clinical trial coordination and/or have equivalent knowledge of FDA regulations and GCPs.

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On-Site and Customized Workshops

CRST offers in-house and customized programs to meet the needs of individual sites. We offer on-site presentations of our regular workshops to enable one or more local sites to provide cost-effective local training for their staff. We can also customize our offerings to meet specialized needs. A prime example is customizing our Basics workshop for investigators.Learn more >