Rosalyn d’Incelli

Vice President, Clinical Operations

Rosalyn d’Incelli joined Sientra in 2009. Ms. d’Incelli has more than 13 years of Clinical Research experience coupled with an accomplished record of clinical achievements. Prior to joining Sientra, she was the Director of Clinical Studies at Mentor Corporation, where she oversaw many of the company’s studies and managed their clinical resources. Ms. d’Incelli was a significant contributor to Mentor’s successful Silicone-Gel PMA approval, and at the time led the company’s large Post-Approval Silicone-Gel study. Additionally, she served as Clinical Director for Mentor’s phase 3 botulinum toxin studies and was previously involved in multiple urology studies. Prior to joining Mentor, Ms. d’Incelli was employed at Inamed Corporation (currently Allergan Medical) in Clinical Operations where she was a member of the clinical study team seeking approval for the company’s Silicone-Gel PMA. She has a demonstrated successful track record in the area of clinical operations with notable clinical studies completions in the areas of Breast and Facial Aesthetics and marketing approvals. Ms. d’Incelli holds a BA from the University of California Santa Barbara and is SoCRA board certified in Clinical Research.