RX for Clinical Trials:
Strategies to Accelerate and Optimize

Bioresearch, pharmaceutical, and CRO organizations have experienced unparalleled growth during the past decade. However the benefits of this growth have also created a new set of business operational challenges that organizations must overcome in order to compete, accelerate profits and improve operating margins.

In addition to managing the complexities of globalization and collaboration with external entities, organizations are being tasked with improving the speed and efficiency of drug development, ensuring drug safety and, in the process, are under pressure to implement industry standards such as CDISC.

Key discussion points will include:

• The benefits of creating a standardized environment for data quality and management; 
• Creating transparency into the path behind your results;
• Leveraging processes to save time through repurposing existing models and reports; and
• Accelerating clinical trials with greater confidence.

Who Should Attend:

• Chief Medical Officers and Medical Directors
• Heads of Medical Affairs and Clinical Research
• Heads of Clinical Operations and Research, Directors and Managers
• VPs and Directors, Scientific Affairs/Government Relations researchers
  CIOs, CTOs, and VPs of Clinical IT
• Heads of Biostatistics, Biometrics, and Data Management
• Clinical Project Leaders and Research Associates
• Clinical/Site Monitors, Auditors, Study Coordinators