Dulce Mariscal
Clinical and Regulatory Affairs Project Lead @Clinical Research Strategies, Llc
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WORK HISTORY
Clinical and Regulatory Affairs Project Lead @Clinical Research Strategies, Llc
Pittsburgh, PA, US
I oversee clinical trials from initiation through to completion in accordance with contracted services with clients. My responsibilities encompass a range of clinical and regulatory duties, particularly ensuring that the clinical trial adheres to all pertinent regulations, including current Good Clinical Practices (GCPs), as well as the standard operating procedures (SOPs) of the company or client.
EDUCATION
University of Pittsburgh
Doctor of Philosophy - PhD, Bioengineering and Biomedical Engineering
Universidad del Turabo
Bachelor's degree, Mechanical Engineering
SKILLS
ABOUT DULCE MARISCAL
Neuroscientist and Clinical Research Professional with expertise in neural engineering, medical device development, and clinical trial operations. Experienced in leading cross-functional clinical and regulatory teams, and optimizing study processes to meet FDA and ISO standards. Proven success in managing NIH- and NSF-funded research projects and translating technical innovation into regulatory and clinical solutions. Passionate about leveraging data and emerging technologies to advance life sciences R&D and improve patient outcomes.
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