Kedrion Biopharma - USA
Jasmine (Irby) Woods, MS, currently serves as a Global Clinical Study Manager and Global Medical Operations Manager at Kedrion Biopharma since April 2021, where responsibilities include managing various trackers, supporting contractor collaborations, and overseeing departmental trainings. Prior experience includes positions as Project Manager at Catalent Pharma Solutions, Associate Program Manager at Syneos Health, and Associate Project Leader at Duke Clinical Research Institute, focusing on project coordination, stakeholder communication, and document management. Jasmine has also held roles at Worldwide Clinical Trials, VWR/Novartis Vaccines, and Multipharma Group, enhancing expertise in clinical operations, procurement, and project management. Academic qualifications include a Master of Science in Clinical Trial Science (Regulatory Affairs) from Rutgers University and a Bachelor of Science in Public Health from Montclair State University.
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Kedrion Biopharma - USA
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Kedrion Biopharma launched US operations in 2011, but the company’s international roots stretch back several decades in the production of blood and plasma-derived products. It places a high value not only on the welfare of those who benefit from its products but also on the people and communities it serves. For more information please visit https://www.kedrion.us/about-us/.