Patricia Mieses
About Patricia Mieses
Patricia Mieses is a Senior Clinical Trial Manager at Bristol Myers Squibb with extensive experience in clinical research and a background in medicine.
Company
Patricia Mieses is currently employed at Bristol Myers Squibb as a Senior Clinical Trial Manager. She works remotely in this role. Prior to this position, she served as a Clinical Trial Manager at Bristol Myers Squibb from 2020 to 2023.
Title
Patricia Mieses holds the title of Senior Clinical Trial Manager at Bristol Myers Squibb. Her responsibilities likely include overseeing clinical trial operations, ensuring compliance with regulatory requirements, and managing study timelines.
Education and Expertise
Patricia Mieses earned a Master of Science in Health Sciences (MSHS) from The George Washington University School of Medicine and Health Sciences in Clinical Research Administration (2017-2020). She also holds a Doctor of Medicine (MD) degree from Pontificia Universidad Católica Madre y Maestra, where she studied General Medicine (2004-2010). Mieses is certified as a Clinical Research Professional (CCRP) by the Society of Clinical Research Associates (SOCRA).
Background
Before her current role, Patricia Mieses held various positions in clinical research and medical fields. She worked as an Associate Clinical Trial Manager at Ferring Pharmaceuticals, a Global Strategic Marketing Consultant at Ethicon, Inc., and a Senior Clinical Research Coordinator at Englewood Hospital and Medical Center. Her career also includes roles as a Medical Assistant/Scribe, Clinical Research Coordinator, and Internal Medicine Clerkship.
Clinical Knowledge and Skills
Patricia Mieses has expertise across multiple therapeutic areas, including interventional cardiology, vascular disease, podiatry, infectious disease, oncology, nephrology, endocrinology, anesthesiology & critical care, wound closure, maternal health, and gastroenterology. She possesses advanced capabilities in Excel for data extraction, management, and analysis. Mieses is proficient with various clinical trial databases and systems such as Medidata Rave, Oracle Clinical, ClinPhone, InForm, REDcap, Veeva Vault, and many others. She has thorough knowledge of ICH/GCP guidelines and federal/international regulations.