This web seminar is designed for sponsor/CRO personnel responsible for protocol design and development, country allocation, site selection, and study feasibility assessments. The current study feasibility assessment process is inefficient and is incapable of identifying the best investigative sites to conduct a clinical trial. Feasibility questionnaires and the current process are often not effective in predicting site success in implementing a given clinical trial. This session will explore novel approaches and technologies that can be used to significantly improve the feasibility assessment process at the protocol, country, and site level.
- Evaluate the traditional approach to study feasibility assessment
- Examine what’s working, what’s not, and why not
- Re-define the concepts of study feasibility at the protocol, country and site level
- Discuss the purpose and objectives for conducting feasibility assessments
- Explore paradigm shifts in the approach and methods for evaluating study feasibility
- Examine a live demonstration of several new methods, technologies, and approaches
- Identify the characteristics of a high-enrolling site for a given study
- Identify how a protocol can be optimized for enrollment and how the sponsor can maximize enrollment at each site
- Employ practical, statistical, and simulation based methods for country allocation and site selection practices
- Directors of Clinical Operations
- Regional Medical Directors
- Clinical Project Managers
- Site Selection Specialists
- Clinical Research Associates
- Clinical Research Associate Managers
Beth D. Harper, B.S., M.B.A.
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Includes up to 20 participants at one site. All participants (up to 20) are eligible for “Certificates of Attendance,” and accreditation, provided that accreditation requirements are met. For groups larger than 20 or for additional sites, please call +1 781.972.5400 or toll-free in the U.S. 800.856.2556 for pricing.
*For individual participants, this web seminar qualifies for a reduced individual participant fee of $349. To register, +1 781.972.5400 or toll-free in the U.S. 800.856.2556.
Barnett International is accredited by the Accreditation Council for Pharmacy Education as a provider of continuing pharmacy education. Participants will receive 2 hours (0.2 CEUs) of continuing education credit for full participation, including the completion of a pre-test, post-test, and program evaluation. Barnett International will issue a receipt of completion for earned CEUs within three weeks of program completion. ACPE#: 0778-0000-14-034-L01-P. Released: 4/14.
Hold this course at your company! For more information, contact Naila Ganatra at +1 215.413.2471.