Recruiting is Critical to Your Success: What is the Secret - Webinar By GlobalCompliancePanel

2 March 2011, Wilmington, United States

Overview: This presentation will go over the steps required for your recruiting process to be successful.

The ability to bring in (recruit) on-time study participants whether they be 'normal healthy adults' or patients with the condition being studied is essential for a CRO, a site, a CPU/CRU for conducting on-time study starts with the full complement of volunteers. For this reason the recruiting process is a top priority of those in management including the PI. The challenges are many but, in the end, it is following the logical steps of the recruitment process that is paramount to a full and on-time study start.

We will go over the challenges that subject recruitment brings and discuss the strategies that you should consider. You will also learn the reasons subjects do and do not participate in clinical trials and why the recruitment phase of a clinical trial is so important. The importance of a good "Recruiting and Community Relations" department eliminates failure as a option.

Why should you attend: Because of the importance of on-time full-panel study starts, it is essential for all members of the study conduct team to be aware of the processes that need to be used to accomplish the goal. Not only is this information useful for CRO's, the sponsors must also know what is needed so they can chose the right CRO or research site to conduct their studies.

Areas Covered in the Session:

* How to set up and track your recruiting of subjects
* The challenges of successful recruiting
* The importance of your recruiting staff in the overall success of the unit or site
* How to build a data-base of patients
* How to recruit more efficiently for a target study
* Factors involved in getting "On-Time Full Panel" study starts
* The four major steps in the recruitment process and the importance of each

Who Will Benefit: This Webinar will provide invaluable assistance to investigators and their staff in the regulatory / legal responsibilities and also the ethical considerations in pharmaceutical product (Drug or device) research involving human subjects. Those benefiting the most would be:

* Principal Investigators and sub investigators
* Clinical Research Scientists (PKs, Biostatisticians, ...)
* Safety Nurses
* Clinical Research Associates (CRAs) and Coordinators (CRCs)
* Recruiting staff
* QA / QC auditors and staff
* Clinical Research Data managers

Price List:
Live : $245.00
Corporate live : $995.00
Recorded : $295.00
Online Training Webinar

Online Training Webinar, 1000 N West Street | Suite 1200, Wilmington, 19801, United States

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