Tracey Becca

Tracey Becca has a diverse professional background in regulatory compliance, clinical trials, and project management across various organizations. At CID Research Institute, Tracey served as a Regulatory Compliance specialist, while an investigation specialist role at Amazon.com involved overseeing fulfillment processes. Tracey contributed as a Clinical Trials Associate at Dendreon and later excelled as a Senior Clinical Documentation Specialist at Seattle Genetics. Following this, Tracey worked as an EHS Documentation Specialist at Bristol-Myers Squibb before taking on the role of Project Coordinator III at Meta, focusing on eye tracking research for Oculus Quest 2, which included responsibilities such as IRB submissions, participant data management, and overall project management coordination. Prior experience at Moffitt Cancer Center involved affiliate research data management.