Susan Keov
About Susan Keov
Susan Keov is a Clinical Research Manager at BeiGene with over 15 years of experience in the clinical research industry, specializing in various therapeutic areas and study platforms.
Current Role at BeiGene
Susan Keov holds the position of Clinical Research Manager at BeiGene. In this role, she oversees clinical research activities and manages a team of Clinical Research Associates (CRAs) across the Australia-New Zealand (ANZ) region. Her responsibilities include coordinating trials, ensuring compliance with Good Clinical Practice (GCP) standards, and supervising the progress of various studies from initiation to completion.
Professional Experience
Susan has a rich professional background with over 15 years in the clinical research industry, spanning various roles. Prior to her current role, she served as Associate Clinical Research Manager, and Associate Manager, Clinical Operations at BeiGene. Her earlier career includes positions such as Clinical Operations Lead at Syneos Health and Senior Clinical Research Associate at inVentiv Health Clinical. She also has experience as a Clinical Research Associate and Research Assistant at PPD and served as a Clinical Trial Coordinator at Monash Alfred Psychiatry Research Centre.
Educational Background
Susan Keov earned her Bachelor of Science degree from RMIT University, completing her studies between 2001 and 2003. Her academic foundation has been instrumental in equipping her with the scientific knowledge necessary for a successful career in clinical research. Over the years, she has continually updated her skill set to keep pace with advancements in the field.
Expertise in Therapeutic Areas
Throughout her career, Susan has gained extensive experience across multiple therapeutic areas, including oncology, nephrology, psychiatry, cardiology, respiratory, rheumatology, and pediatrics. This diverse exposure has enabled her to effectively manage a variety of clinical trials across different medical specializations.
Technical Proficiency
Susan brings proficiency in various study platforms crucial for clinical research. Her technical skills encompass Electronic Data Capture (EDC), Clinical Trial Management Systems (CTMS), electronic Trial Master Files (eTMF), and Interactive Voice/Web Response Systems (IVRS/IWRS). These competencies ensure the seamless execution and management of clinical trials.