Mscr Sase Boyo
About Mscr Sase Boyo
Mscr Sase Boyo is a Clinical Project Manager with over 13 years of experience in clinical operations and monitoring of global clinical trials. She has held various roles in organizations such as PPD, Morehouse School of Medicine, and Nutrasource, where she manages clinical resources and oversees budgets and timelines for clinical studies.
Work at Nutrasource
Mscr Sase Boyo has been serving as a Clinical Project Manager at Nutrasource since 2016. In this role, she oversees clinical resources to ensure alignment with ongoing clinical activities. Her responsibilities include managing budgets and timelines for risk assessment and mitigation in clinical studies. She has contributed to maintaining the forward movement of clinical deliverables, demonstrating her expertise in clinical operations.
Education and Expertise
Mscr Sase Boyo holds a Master's degree from Morehouse School of Medicine, which she obtained between 2009 and 2011. She also earned a Bachelor's degree in Biology from California State University, Northridge, from 2000 to 2005. Additionally, she studied Public Administration and Management at Kennesaw State University, completing her Master's in 2008. With over 13 years of experience in clinical operations and monitoring of global clinical trials, she possesses extensive knowledge in the field.
Background
Mscr Sase Boyo has a diverse professional background in clinical research and project management. She began her career as a Drug Safety Assistant and Quality Assurance Associate at UCB, Inc. in 2006. Following this, she worked as a Clinical Research Associate at Clinical Pharma Services Ltd in the UK from 2007 to 2009. She has held various roles, including Clinical Trial Coordinator at Amgen and Clinical Research Associate at PPD, where she worked for nine months before transitioning to a Clinical Team Manager role in 2019.
Achievements
Throughout her career, Mscr Sase Boyo has been recognized for her skillful utilization of resources to establish priorities, schedule, and meet deadlines. Her role as Clinical Team Manager at PPD involves the implementation and training of standardized clinical monitoring processes within study teams. She has successfully managed clinical resources and ensured alignment with clinical activities, contributing to the success of various clinical studies.