2nd Annual Clinical Site Feasibility, Selection, and Startup

Share |

 

 

Why You Should Attend This Conference?

  • High Level Speaking Faculty
  • Lessons Learned From Three Case Studies
  • Enhanced Interactivity and Engagement Through Roundtable and Panel Sessions
  • Improved Opportunities for Networking Through Tri-located Event
  • Presentations that Focus on Concrete Strategies for Improving Quality While Reducing Trial Delays and Costs

Speakers Include:

Heather Almonte, Associate Director, Clinical Operations, OCTAPHARMA
John Burnett, Senior Clinical Trial Manager II, EXELIXIS
Chris Conklin, Global Trial Optimization, MERCK & CO
Karen Carroll, Director, Clinical Site Services, VERTEX PHARMACEUTICALS
Jenneen DeFiore, Global Patient Recruitment Specialist, ROCHE
Christina DiArchangelo, CEO, ARMONIA CLINICAL RESEARCH, LLC
Daniela Franschman, Manager, Global Trial Optimization, MERCK & CO
Lani Hashimoto, Director, Strategic Development, MMG
Lisa LaLuna, Senior Vice President Corporate Development & Implementation, ePHARMASOLUTIONS
Shae Owens, Regulatory Affairs Coordinator, KOOTENAI CANCER CENTER
Raymond Panas, PhD, Director of International Clinical Development, SUCAMPO
Ross Pettit, Vice President, Clinical Operations, AMAG PHARMACEUTICALS
Frank Plonski, Clinical Project Manager, PFIZER
Joe Popowicz, Associate Director, Clinical Operations, ORTHOVITA
Alexandra Poulos, Manager, External Partnerships, RPS
Richard Robinson, Assistant Director, Diabetes and Metabolism Group, SANOFI-AVENTIS
Lakisha Rodwell, Global Trial Optimization Specialist, MERCK & CO
Miriam Verduzco, Director, Patient Recruitment and Site Management Services, ALLERGAN
Howard Waxman, Director of Research, BELMONT CENTER FOR COMPREHENSIVE TREATMENT
Jeffrey Zucker, Senior Director and Global Head, Patient Recruitment, KENDLE


JUSTIFY YOUR TRIP!
If you have to first convince your boss it’s worth your time and the company’s money to go, you’re not alone. Past conference attendees have helped us create justification documents 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

This Summit is specifically designed for C-Level Executives, Department Heads, Vice Presidents, Directors, and Managers at Pharmaceutical, Biotechnology, and Medical Device companies from the following departments:

  • Clinical Operations
  • Clinical Research/Development
  • Trial Optimization
  • Site Selection
  • Protocol Feasibility
  • Investigator Recruitment
  • Patient Enrollment/Recruitment
  • Site Monitoring/Management
  • Clinical Data Analyst/Informatics Analyst
  • Clinical Quality Assurance
  • Clinical Project/Study Managers
  • CRA’s
  • Regulatory Affairs
  • Medical Affairs



This conference is also of interest to Senior Level Representatives from Sites and Representatives responsible for Feasibility, Site Selection, Trial Optimization, and Patient Recruitment at CRO’s.