Evelyn Rivera
About Evelyn Rivera
Evelyn Rivera is a Clinical Manager at Bristol-Myers Squibb and a Sr. IHCRA at Novo Nordisk, with extensive experience in managing clinical trials for cardiovascular, dermatological, and gastrointestinal disorders.
Current Roles and Responsibilities
Evelyn Rivera is currently serving as a Clinical Manager at Bristol-Myers Squibb in the United States. She also holds the position of Senior IHCRA at Novo Nordisk in Princeton, NJ. Aside from her roles in the healthcare industry, she also works as a Public Notary in New Jersey. These positions highlight her extensive expertise and active involvement in the clinical and healthcare sectors.
Educational Background
Evelyn Rivera has a robust educational background. She holds a Postgraduate certificate from Edinburgh Napier University, which she completed in one year from 2008 to 2009. Additionally, she studied at Robert Wood Johnson Hospital for 11 months in 2006 and spent a year at The College of New Jersey from 2003 to 2004. She earned her Bachelor's Degree (BS) from Universidad de Puerto Rico, where she studied from 1996 to 2002. Prior to that, she completed her high school education at Colegio Bautista de Caguas from 1994 to 1996.
Clinical Expertise and Specializations
Evelyn Rivera has specialized expertise in managing clinical trials for a variety of medical conditions, including cardiovascular diseases, dermatology, and gastrointestinal disorders. Her knowledge extends to treating complex skin and skin structure infections, covering both gram-positive and gram-negative infections. She is well-versed in overseeing clinical studies for congestive heart failure and coronary artery disease. Her experience also encompasses handling clinical trials for chronic ailments such as gout and bowel disease.
Experience in Clinical Site Management
With over seven years of experience in clinical site management, Evelyn Rivera has developed strong capabilities in overseeing the logistics and operations of clinical sites. Her role involves coordinating clinical trials, ensuring compliance with regulatory standards, and maintaining high levels of data integrity. This extensive experience underscores her proficiency in managing clinical sites efficiently and effectively.