Yvonne Converso-Baran
Senior Director, Quality Assurance, Americas @Syneos Health
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WORK HISTORY
Senior Director, Quality Assurance, Americas @Syneos Health
Ann Arbor, MI, US
Syneos Health\" is the only fully integrated biopharmaceuticals organization. Our company, including a Contract Research Organization (CRO), and Contract Commercial Organization (CCO), is purpose-built to accelerate customer performance to address modern market realities. Created through the merger of two industry leading companies- INC Research and inVentiv Health- we bring together more than clinical and commercial minds with the ability to support customers in more than 110 countries. Together we share insights, use the latest technologies and apply advanced business practices to speed our customers\' delivery of important therapies to patients. In short, we are shortening the distance from lab to life.
EDUCATION
UMass Boston
Biotechnology, Masters Program
University of Detroit Mercy
Bachelor of Science, Biology/Biological Sciences, General
ABOUT YVONNE CONVERSO-BARAN
RQAP-GCP. I have 20+ years industry experience in pharma research, starting with 6.5 years at a small radiopharmaceutical start up, as a CRA, Clinical Operations Manager, including managing 3 concurrent Phase 3 trials and Manager of the Imaging Lab. I also have 16 yrs at one CRO, in Project Management, Clinical Operations (responsible for Clinical Study Start Up, CTMS, files management, and in house trial monitoring), Drug Safety and Quality Assurance (12 years). Currently a Senior Director in Quality Assurance, supervising a staff of auditors, providing auditor training and mentoring, resourcing, process improvements, subject matter expert on Pharmacovigilance issues, root cause analysis, escalated quality issues and audits (process and client), facilitate regulatory inspections, provide management review of audit reports and CAPAs. I am also SQA certified in GCP.Prior to this, my background is in Nuclear Medicine (Molecular Imaging), where I spent 10+ years working in clinical nuclear medicine, including 3 years as the lead performing radiopharmaceutical clinical trials.
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