Learn about the latest trends affecting biopharma R&D including, study diversity & transparency, predictive feasibility and more...
Watch Ms. Branon’s lively presentation and discover how central access to one comprehensive source for relevant, timely clinical trial data and trial benchmarks vastly improves your study planning and feasibility processes.
Becoming the “expert to the experts” for your pharma and CRO clients
Using data from the newly redesigned Citeline suite of intelligence tools, Ms. Branon, a member of the Citeline team for over 10 years and Director of Sitetrove, will use her expertise to elucidate the connection between leveraging top-quality intelligence and becoming the “expert to the experts” for your pharma and CRO clients. With her years of experience in the field, especially in site feasibility, staff management, and helping clients develop strategies to identify the most experienced investigators and trial sites, Ms. Branon’s insights are sure to enlighten.
Citeline, Sitetrove: Clinical trial site & investigator iden...
Even one misstep in your clinical trials strategy or execution can cost your company millions. Save time and cost with the trusted source for global investigator and site intelligence and global pharmaceutical clinical trial intelligence by subscribing to Sitetrove and Trialtrove.
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