Trialstat Appoints Deidre Redmond to Vice President Clinical Affairs

Trialstat Appoints Deidre Redmond to Vice President Clinical Affairs










Ottawa, ON (PRWEB) September 22, 2006

TrialStat Corporation (http://www.trialstat.com), a clinical data management on demand company, today named Deidre Redmond to the position of Vice President Clinical Affairs. Ms. Redmond has more than 20 years of clinical research experience in addition to a number of years as a registered nurse in the areas of critical care and oncology. Her primary role at TrialStat will be to guide the development of ClincialAnalytics (CA) 3.0(tm), the company’s on demand EDC platform, and data management services to ensure they remain innovative, effective and standards compliant.

“Deidre’s comprehensive knowledge and breadth of clinical research experience will enhance TrialStat’s ongoing focus on delivering highly effective clinical data management solutions for our customers,” said Jonathan Barker, President and CEO, TrialStat. “Deidre has a customer perspective on EDC and data management that will be invaluable as we continue rapid expansion in our U.S. and European markets.”

Prior to joining TrialStat, Ms. Redmond managed Canscot Clinical Research, an independent consultancy specializing in clinical trial management services for pharmaceutical and biotechnology companies and contract research organizations. Her extensive clinical research experience encompasses the full clinical trial lifecycle, from study start-up to regulatory submission. This expertise also includes project management, site training, quality assurance and compliance audits, clinical study rescue and FDA audit preparation and resolution.

“Clinical research organizations are looking for new approaches to cost-effectively streamline the collection and management of trial data in order to reduce time-to-market for new drugs and treatments,” said Ms. Redmond. “TrialStat’s ability to integrate its ClinicalAnalytics EDC platform with its data management services offers research organizations an optimal on demand solution that lowers costs, speeds clinical trial implementation and enhances the quality of research.”

ClinicalAnalytics (CA) is an integrated web and handheld-based EDC solution that enables users to design, configure and manage clinical research projects themselves through a browser interface. This secure, cost-effective approach accelerates project startup, site addition and management, recruitment monitoring, query resolution and final data analysis. TrialStat’s Data Management Services group offers a spectrum of data management services, from biostatistics, data entry, adverse event coding and training to project management among others. These services are available either á la carte or in an integrated suite.

ABOUT TRIALSTAT

Headquartered in Ottawa, Canada, TrialStat is a privately held company that delivers clinical data management on demand by combining its full suite of data management services with the company’s software as a service products. CA 3.0 is a robust and scaleable clinical EDC on demand solution used by leading academic and contract research organizations. SRS 3.0(tm) automates systematic reviews using real-time collaboration and management tools to achieve transparent, auditable and reproducible results quickly and cost-effectively. For more information, please visit us at http://www.trialstat.com.

ClinicalAnalytics 3.0 is a registered trademark of TrialStat Corporation.

SRS 3.0 is a registered trademark of TrialStat Corporation.

For media inquiries, please contact:

Shelley Mullins    

Media Relations, TrialStat    

613-866-8803        

Kathryn Schwab

Media Relations, TrialStat

613-858-4407

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KePRO Promotes Barbara Knox to Vice President, Product Management

KePRO Promotes Barbara Knox to Vice President, Product Management










Harrisburg, PA (PRWEB) July 23, 2011

The Keystone Peer Review Organization, Inc. (KePRO) recently promoted Barbara Knox to the position of Vice President, Product Management. Ms. Knox assumes overall responsibility for directing, planning, and implementing all care management product development objectives.

In her new role, Ms. Knox will develop and implement KePRO’s strategic product development roadmap to maximize the company’s market position and strengthen its growth strategy. “Barbara has proven herself to be a health care market expert during her tenure with KePRO,” said Joseph A. Dougher, chief executive officer. “She will use her expertise to monitor market trends, analyze competitors, and ensure that KePRO’s products help members better manage their health.”

With over 20 years of experience in product development and marketing, Ms. Knox is highly qualified to position KePRO to better meet the needs of health care management clients. “My experience in product development and management, identifying market opportunities, strategic and operational planning, and reengineering and management of operational processes, will help position KePRO to maximize its market presence through innovative fully integrated products that deliver the best return on investment for clients.”

Prior to joining KePRO, Ms. Knox was Vice President of Product Management with SHPS, a health and human resource management company. She was responsible for the implementation of an integrated health management strategy, as well as the development of disease management, utilization management, case management and wellness/health promotion products.

Ms. Knox holds a Masters of Business Administration (MBA) in Marketing from the University of Baltimore and a Bachelor of Science degree in Business Education from Morgan State University. She has received many awards and recognition, including 100 Leading Black Women, Who’s Who in American Women and 100 Leading Black Professional Women.

About KePRO

KePRO, a leading quality improvement and care management organization, offers innovative and outcomes-focused solutions to reduce the utilization of health care resources and optimize quality of care for public and commercial clients. KePRO’s comprehensive, member centric care management solutions go far beyond traditional utilization and case management by coordinating the care provided to members with acute, chronic and complex conditions across the continuum, and identifying members who are at the highest risk for future services, but have not yet had an acute event. Tailored programs maximize members’ quality of life, and realize greater cost savings for members and clients.

Headquartered in Pennsylvania, KePRO also has offices in Florida, Ohio, Tennessee, Texas, and Virginia. KePRO is URAC health utilization management and case management accredited. For more information, visit http://www.kepro.com.

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