Miesha Solomon
About Miesha Solomon
Professional Background
Miesha Solomon is currently employed at Bristol Myers Squibb as a Regulatory Affairs Specialist, leveraging her extensive experience in regulatory submissions and data quality. She has a diverse background in the pharmaceutical industry, ranging from clinical data analysis to project coordination. Her previous roles include working at GSK as a Regulatory Submissions Specialist, Eisai in Global Regulatory Operations, and Sanofi as a Project Manager, among others.
Regulatory Affairs Expertise
Miesha Solomon possesses significant expertise in regulatory affairs, having worked in a variety of roles that involve regulatory submissions, data quality, and standards. Her positions at Bristol Myers Squibb, Sanofi, and Eisai underscore her comprehensive understanding of regulatory operations and compliance within the pharmaceutical industry.
Clinical Research Experience
Miesha Solomon's background includes notable experience in clinical research coordination, particularly during her tenure at Duke University Medical Center. This role equipped her with the knowledge and skills necessary to oversee clinical studies and ensure compliance with regulatory requirements.
Technical Skills in Electronic Publishing
Miesha's stint as an Electronic Publishing Specialist at PPD provided her with specialized skills in the field of electronic publishing. This role involved preparing and submitting electronic regulatory documents, an essential function within regulatory affairs.
Educational Qualifications
Miesha Solomon earned a Bachelor of Business Administration (BBA) in Management from New Jersey City University. Her educational background in business administration complements her professional experience, providing her with strong management and leadership capabilities.