Tamara Dimovski
About Tamara Dimovski
Tamara Dimovski is a Clinical Trial Manager with extensive experience in clinical research, currently working at Arcus Biosciences since 2022. She has held various roles in organizations such as AbbVie, Syneos Health, and Karmanos Cancer Institute, contributing to the management and execution of clinical trials.
Current Role at Arcus Biosciences
Tamara Dimovski has been serving as a Clinical Trial Manager at Arcus Biosciences since 2022. In this role, she is responsible for overseeing clinical trials, ensuring compliance with regulatory requirements, and managing the overall progress of studies. Her duties include coordinating with various stakeholders, including clinical program managers and contract research organizations, to facilitate the timely initiation of trials.
Previous Experience in Clinical Research
Prior to her current position, Dimovski worked at AbbVie as a Clinical Research Associate II from 2019 to 2021. She also held the position of CRA II at Syneos Health on assignment with AbbVie from 2018 to 2019. Her experience includes performing in-house reviews of clinical data listings for accuracy and completeness, as well as escalating issues to the Clinical Program Manager when necessary.
Background in Clinical Research Coordination
Dimovski has a solid foundation in clinical research, having worked as a Certified Clinical Research Coordinator at Karmanos Cancer Institute from 2013 to 2018. She began her career in research as an Undergraduate Research Assistant at the same institute from 2011 to 2012. This background provided her with extensive experience in managing patient enrollment for complex clinical trials.
Educational Qualifications
Tamara Dimovski earned her Bachelor's Degree in Psychology and Health Sciences from Wayne State University, where she studied from 2007 to 2013. Her academic background has equipped her with a strong understanding of the psychological and health-related aspects of clinical research.
Skills in Clinical Trial Management
Dimovski possesses expertise in several key areas of clinical trial management. She supports the development and design of Case Report Forms (CRFs) and participates in the Electronic Data Capture (EDC) and Interactive Voice Response System (IXRS) specification process. Additionally, she assists with the setup of central labs and study vendors, ensuring effective communication and training for site staff.