ClinicalRM to Promote Clinical Research Program Management Expertise at DIA

June 2, 2011, Hinckley, OH - Clinical Research Management, a full-service Contract Research Organization providing expertise in research, trials and regulatory support, announced today it will be exhibiting at the DIA (Drug Information Association) Annual Meeting June 19-23 in Chicago, IL.  On-site will be Jennifer Zimmerer, MS, RD, CCRP, and Program Manager for ClinicalRM to answer questions and share insight into successful program management of research and all phases of clinical trials in both commercial and government sectors.

The complexity and growth of regulatory requirements puts critical pressure on Program Managers to meet competing demands for scope, time, cost, risk, and quality.  “The cost of research and clinical trials is always a significant concern for any organization.  And although you can’t eliminate steps in the program, you can be more efficient and work proactively to ensure the best program outcome for a customer,” said Jennifer Zimmerer.  “Our goal at DIA is to have informative discussions about how optimal program management can effect program demands in positive and negative ways, and share out knowledge with other organizations.”

A cornerstone of ClinicalRM’s success is that its Program Managers also have clinical experience which elevates the ability of its team to anticipate issues or challenges across any program.  Since the company’s inception, its Program Managers have remained highly accessible at customer locations to facilitate communication and teamwork and ensure fiscal accountability.  This approach minimizes the lines of authority and ensures that important decisions can be acted on quickly and appropriately.