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Evan Dubose, PhD

Clinical Research Scientist II

Evan DuBose, PhD is a Clinical Research Scientist II at SynerG Biopharma Group. Prior to joining SynerG Biopharma Group, Evan gained experience in clinical trial development and regulatory affairs at Cato Research (now Allucent) where she worked as a regulatory strategy intern.

Evan has over 5 years of experience in regulatory medical writing and project management. Evan’s regulatory writing experience includes writing CSRs, IBs, and protocols in therapeutic areas which include neurology and immunology. Evan has over 10 years of experience conducting, presenting, and publishing basic medical science and clinical research.

Evan received a BS in chemistry from Spelman College and a PhD from the UNC-Chapel Hill Department of Pharmacology. Evan’s dissertation work focused on identifying novel treatment modalities for metastatic melanoma to overcome intrinsic and extrinsic resistance to current therapies. In her time away from work, she enjoys crafting and traveling. She also loves attending basketball and baseball games.

Evan Dubose, PhD's Recent Articles

Prescription for Success: Streamlining Meetings to Craft Compelling Regulatory Documents

February 29, 2024 | Evan DuBose, PhD and Kelsey Gray, PhD – Clinical Research Scientists | Medical Writing Services   Does scheduling meetings feel like a circus act between juggling multiple calendars and balancing competing priorities? If so, you will…

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