Topstone Research
Natalie White is an accomplished clinical research professional with extensive experience in monitoring clinical sites and conducting evaluations at various trial stages. Currently serving as a Clinical Research professional at DOCS since 2018 and as a Clinical Research Associate at Topstone Research since January 2016, Natalie has a robust background that includes positions as a Clinical Research Associate at genae associates nv and HAMPTON KLARKE, where responsibilities included reviewing trial protocols, monitoring site activity, and conducting staff training. Earlier experiences include working as a Clinical Research Coordinator at BAY RESEARCH and as a Chemist at Sigma-Aldrich. Natalie holds a Bachelor of Science degree in Biology and Chemistry from Montclair State University, earned between 1997 and 2003.
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Topstone Research
Rely on Topstone Research for Effective Clinical Trial Management In clinical research, complex challenges are more of a rule than an exception. Choose a provider whose expertise and execution can help you simplify the moving parts of clinical study conduct and manage the challenges that inevitably occur through the life of a trial. We have both the staff experience and resources to effectively and successfully deliver what is promised – expedient and compliant Phase I-IV clinical research studies over a range of therapeutic areas. Therapeutic Expertise Our collective expertise in different therapeutic fields offers you insights into the practicalities and pitfalls that impact the conduct of any trial. Topstone’s clinical professionals bring in-depth experience in a variety of key therapeutic areas, including allergy, respiratory, vaccines, dermatology, cardiovascular, central nervous system, endocrinology, oncology and pain management. Site Support to Boost Performance Site performance is the lifeblood of clinical trial success. Within its own network, Topstone has more than 30 investigator sites with access to more than 500,000 patients. Managed fully by Topstone’s clinical staff, these sites operate with centralized SOPs and harmonized training. For other sites, we offer a menu of start-up services and an extra layer of clinical research infrastructure support to sites who need additional resources.