Staff to Lead Teams Focused on Project Management, Data Management and Bio-statistical Services for Medical Device Clinical Trials
NORTH ATTLEBORO, Mass., Feb. 5 /PRNewswire/ -- MDCI, a full-service CRO serving the medical device industry, today announced the following staff promotions in its Clinical Services group, effective immediately.
Kristine Bello, MPH has been promoted from senior clinical project manager to associate director of clinical project management. In this new role Kris will be responsible for overseeing the clinical services project management function while streamlining the department's processes for maximum efficiency and customer satisfaction. Karin E. Graefe has been promoted from senior clinical data manager to associate director of clinical data management and will be responsible for leading the clinical trial data management group, ensuring MDCI will continue to provide state-of-the-art data services to meet the industry's changing needs. Laiju Zhang, Ph.D has been promoted to senior manager of biostatistics and SAS programming and will be responsible for expanding MDCI's biostatistics and SAS programming services to benefit clients through all phases of clinical trial execution, from study design through data management, to the statistical analyses of the clinical data.
"I am very pleased to announce the promotions of these experienced and talented professionals," said Leslie Rose, MDCI's director of clinical services. "Each of these individuals brings specialized knowledge in their respective areas. They will lead high-performing and skilled teams to help our clients successfully and effectively design, manage, and analyze their medical device clinical trials."
About Medical Device Consultants, Inc. (MDCI)
MDCI is a full-service consulting firm and contract research organization (CRO) that helps emerging and established companies commercialize novel and innovative medical devices, diagnostics, and combination products. MDCI has helped hundreds of clients conduct successful clinical trials, achieve regulatory clearance and approval, and maintain compliance for products in the U.S. and internationally. The company has offices in Massachusetts, California, and London. For more information, visit http://www.mdci.com
|SOURCE Medical Device Consultants, Inc.|
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