Demetria Collins
About Demetria Collins
Demetria Collins is a Senior Clinical Trial Manager at Bristol Myers Squibb with over 20 years of clinical research experience, including 12 years of industry monitoring.
Company
Demetria Collins currently works at Bristol Myers Squibb as a Senior Clinical Trial Manager in a remote position. Bristol Myers Squibb is a global biopharmaceutical company known for its commitment to discovering, developing, and delivering innovative medicines that help patients prevail over serious diseases.
Title
Demetria Collins holds the title of Senior Clinical Trial Manager. In this role, she oversees and coordinates clinical trials to ensure compliance with regulatory requirements and clinical trial protocols. Her responsibilities include managing timelines, budgets, and resources to ensure successful trial outcomes.
Education and Expertise
Demetria Collins earned her Bachelor of Science degree in Biology from Roosevelt University, where she studied from 1992 to 1996. She has over 20 years of clinical research experience, including 12 years of industry monitoring. Collins is fully proficient in ICH/GCP, FDA Guidelines, Microsoft Office, Medidata, Inform, Bioclinica, and CTMS.
Background
Demetria Collins began her career in clinical research at the University of Chicago in 1996, where she worked as a CRA/Transplant Coordinator/QA for nine years. She gained experience in various roles across notable organizations such as Quintiles, ReSearch Pharmaceutical Services, and MannKind Corporation. Her extensive background includes positions as an Independent CRA and Senior Clinical Research Associate at Execupharm, ICON plc, PPD, PRA Health Sciences, and Self Employed.
Clinical Research Experience
With over 20 years of clinical research experience, Demetria Collins has amassed significant expertise in monitoring clinical trials from Phase I-IV. Her industry experience began in 2006, and she has worked with various contract research organizations (CROs) and pharmaceutical companies. Collins has practical and working knowledge of all duties related to clinical trial monitoring and is particularly interested in helping to propel the approval of new treatments and therapies.