Quality Assurance at the (Clinical Research) Site: How to Develop a Manageable Plan

This clinical compliance training will help attendees understand how they can develop and implement a Quality Assurance (QA) program at their clinical research site that ensures the staff are properly trained and that the research is carried out in accordance with regulatory expectations.

Why Should You Attend:

Is your site carrying out clinical research in accordance with regulatory expectations? You have training requirements for investigators and coordinators, is that enough? Is it worthwhile training that covers necessary topics? A Quality Assurance (QA) Program is the vehicle to help you answer these questions and more.

Who Will Benefit:

This webinar will provide valuable assistance to following personnel:

Experienced Clinical Research Coordinators

Experienced Principal Investigators

Experienced Clinical Research Associates (Monitors)

Site Based Clinical Research Managers and Administrators

Instructor Profile:

Jennifer Holcomb, MA, CCRC, is a clinical research professional with over 20 years of experience in the field. Currently employed by UCHealth Systems, (jennifer.holcomb@uchealth.org), she provides guidance and leadership in the establishment and development of policies in the conduct and management of clinical research. 

Note:

Use coupon code NB5SQH8N and get 10% off on registration.

For Registration:

http://www.complianceonline.com/quality-assurance-at-the-clinical-research-site-webinar-training-702406-prdw?channel=sciencedz