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Rebecca Sandahl

Study Start-Up Team Manager at PPD

Rebecca Sandahl is a seasoned professional with a strong background in clinical and biomedical research.

Her expertise includes designing, managing, and ensuring compliance of clinical studies across academic, government, and industry sectors.

With over five years of experience in clinical research and ten years in biomedical research, Rebecca has a wealth of knowledge in the field.

She has a specialized focus on neurobiology and is well-versed in pharmacogenetic, molecular biology, and behavioral research.

Rebecca holds a Ph.D. in Neurobiology from UNC Chapel Hill and a Bachelor of Arts in Biology/Biological Sciences from Cornell University.

Her professional journey includes roles such as Study Start-Up Team Manager, Principal Country Approval Specialist, and SIA Team Manager at PPD.

Prior to this, she served as a Postdoctoral Research Fellow at the National Institute on Alcohol Abuse and Alcoholism (NIAAA, NIH) and as a Clinical Research Coordinator at Massachusetts General Hospital.

Rebecca's diverse experience also extends to her time as a Graduate Student at the University of North Carolina at Chapel Hill and as a Medical Intern at Purdue Pharma L.P.

Her skill set encompasses the development and management of regional study start-up and regulatory submission plans for multi-national clinical trials.

Rebecca Sandahl
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Location

Raleigh, North Carolina, United States