Scott Brown, PhD

Scott Brown, PhD

Biostatistician Scott has 18 years of experience in biostatistics for clinical trials, covering a wide variety of therapeutic areas including cardiovascular, neurological, urological, peripheral vascular and orthopedic. He was previously head of biostatistics for...
Lisa Gallatin, RAC

Lisa Gallatin, RAC

Regulatory Consultant Lisa brings over 15 years of regulatory experience to BRIGHT and assists clients in the development and execution of thoughtful, creative, and efficient regulatory strategies and market authorizations. Through her work at various-sized medical...
Robin Solinsky, CCRP

Robin Solinsky, CCRP

Clinical Research Consultant Robin crossed over into clinical research after a few years as a quality engineer at Abbott (formerly St. Jude Medical). She has worked on all aspects of clinical trials across a multitude of companies, ranging from small start-ups to...
Mary Ovick

Mary Ovick

Clinical Research Consultant Mary is an operations and project management professional with over 9 years of clinical research experience. Mary is highly proficient in clinical trial start-up management, process development and documentation, MS Access database...
Hannah Bearinger, PhD

Hannah Bearinger, PhD

Clinical Research Consultant Hannah has experience in biomaterials research, medical device product development, and working with start-up companies. Always eager to learn, she joined the BRIGHT team as a utility player to help with business development, technical...