7th Annual Clinical Performance Metrics & Benchmarking Summit

ExL Pharma’s 7th Annual Clinical Performance Metrics & Benchmarking Summit provides professionals with the right knowledge and tools to drive improved performance and efficiency of clinical development. This event focuses on establishing appropriate performance measures to allow benchmarking of clinical trials efficiency and productivity. As well, this event teaches attendees developing mechanisms for ongoing data collection in order to facilitate and support clinical research. This allows proper comparisons to be made with other clinical trials destinations and individual companies' performance over time.

The 7th Annual Clinical Performance Metrics & Benchmarking Summit is co-located with ExL Pharma’s 3rd Annual Clinical Budgeting & Contracting conference. These two events will share coffee breaks, continental breakfast, and lunch, which allows for increased networking opportunities filled with senior-level professionals which helps build relationships through memorable and relevant shared experiences.

 

Attendee Profile

Company Profile

 

Top Five Reasons to Attend This Conference

  1. Maximizing your clinical trial performance by bridging the gap between identifying and implementing metrics
  2. Best practices on processing data and on-site performance to improve patient recruitment and study time
  3. Hearing an investigators perspective on working with a sponsoring company that uses metrics and how it affects the relationship
  4. Keynote presentation on leveraging metrics to improve organizational performance
  5. This event is being co-located with ExL Pharma’s 3rd Global Clinical Budgeting & Contracting conference. These two events will share networking breaks and lunch with senior-level professionals, which helps build networking relationships through memorable and relevant shared experiences.

Don't miss your chance to hear from our most recently added session:

BENCHMARKING CASE STUDY

  • Identifying benchmarking trials
  • Extracting and calculating critical benchmark parameters: patients, sites, enrollment period, randomization rate, screen fail rate
  • Estimating modeling parameters and risk/ uncertainty
  • Predicting and assessing clinical trial performance: site performance, cycle times, opportunities for improvement

Michael Lonetto, GTO Informatics Specialist, MERCK

 

JUSTIFY YOUR TRIP!

If you have to first convince your boss it’s worth your time and the company’s money to attend this event, you’re not alone. Past conference attendees have helped us create the following justification document that will let you make your case on why this is a must-attend conference for you. Feel free to download and customize the letter below as you see fit, adding immediate problems you’ll be able to solve and long-term initiatives you’ll be able to implement. Chances are good you’ll be able to do those things and more after the conclusion of our 2011 event!

CLICK HERE TO DOWNLOAD OUR JUSTIFICATION PROPOSAL

Who Should Attend

Professionals from pharmaceutical, biotechnology and medical device companies with responsibilities in the following departments:

  • Process Improvement/Enhancement
  • Metrics and Benchmarking Development
  • Performance Management
  • Clinical Operations
  • Clinical Development
  • Clinical Planning
  • Clinical Trials
  • Clinical Studies
  • Resource Management
  • Research & Development Operations
  • Research & Development Development
  • Data Management
  • Project Management
  • Project Planning
  • Process Planning
  • Medical Affairs
  • Business Development/Operations
  • Strategic Development
  • Technology Development
  • Capacity Planning/Management
  • Drug Development and Safety Management
  • Regulatory Development

 

This program is also of interest to:

  • CROs (Clinical research organizations)
  • Technology (systems used for acquiring, implementing and maintaining data)
  • Other Services/Consultancies