Taryn Rupinta
About Taryn Rupinta
Taryn Rupinta is a Senior Clinical Trial Manager with over a decade of experience in the biotechnology and pharmaceutical industry, specializing in clinical trials management. She holds a Master's Degree in Public Health from Johns Hopkins Bloomberg School of Public Health and has worked at various organizations, including Biogen Idec and QuintilesIMS.
Work at Inozyme
Taryn Rupinta currently serves as a Senior Clinical Trial Manager at Inozyme Pharma, a position she has held since 2022. In this role, she is responsible for overseeing clinical trials, ensuring compliance with regulatory requirements, and managing study timelines. Her experience in clinical trial management allows her to effectively prioritize multiple demands across several studies, consistently meeting and exceeding sponsor and study team expectations.
Education and Expertise
Taryn Rupinta holds a Master’s Degree in Public Health from Johns Hopkins Bloomberg School of Public Health, which she completed from 2017 to 2021. She also earned a Bachelor of Science in Public and Community Health from the University of Maryland, studying from 2004 to 2008. Additionally, she achieved a Certificate in Entrepreneurship Essentials from HBX | Harvard Business School in 2018. Her educational background supports her extensive experience in the biotechnology and pharmaceutical industry.
Background in Clinical Trials
Taryn Rupinta has over a decade of experience in the biotechnology and pharmaceutical industry, specifically in clinical trials management. She has held various positions, including Clinical Trial Assistant at QuintilesIMS and Sr. Clinical Trial Associate at Centrexion Therapeutics Corp. and C4 Therapeutics, Inc. Her roles have involved collaborating with international team members and stakeholders, demonstrating strong professional communication skills.
Previous Work Experience
Throughout her career, Taryn Rupinta has held multiple positions in clinical trial management and related fields. She worked at Biogen Idec as a Patient Data Coordinator and Patient Services Coordinator from 2012 to 2014 and 2009 to 2012, respectively. Other notable positions include Document Specialist-QC at MedImmune and Associate Clinical Trial Lead at Torque. Her diverse experience contributes to her proficiency in managing clinical trials effectively.
Professional Development
Taryn Rupinta is committed to continued learning and professional development. She actively seeks opportunities to enhance her skills and knowledge within the clinical trials field. Known for her ability to adapt to updated procedures with professionalism and accuracy, she ensures high-quality work while meeting deadline expectations across various studies.