Ryoko Oka
About Ryoko Oka
Ryoko Oka is a Clinical Trial Oversight Manager at BeiGene in Sydney, Australia, with extensive experience in clinical research and data management.
Title
Ryoko Oka serves as the Clinical Trial Oversight Manager at BeiGene in Sydney, Australia. With a focus on effectively managing clinical trials, she ensures that all stages from site selection to close out are meticulously executed.
Background in Clinical Research
Ryoko Oka began her career in clinical research at CRC Research in Vancouver, British Columbia, where she completed an internship in 2011. She then joined EPS Corporation as a Data Management professional in Osaka, Japan, from 2010 to 2011. Between 2011 and 2015, she worked at ICON plc in Osaka as a Clinical Research Associate (CRA). From 2015 to 2020, Oka served as a CRA at PRA Health Sciences in Sydney. Her varied roles have equipped her with a broad understanding of clinical research operations.
Experience with Global Multi-National Sponsored Trials
Throughout her career, Ryoko Oka has managed all types of onsite visit types for numerous global, multi-national sponsored trials. Her broad expertise spans from site selection to close out. She excels in adaptive monitoring techniques, including offsite monitoring, ensuring comprehensive oversight and compliance in clinical trials.
Therapeutic Area Experience
Ryoko Oka has accumulated extensive therapeutic area experience in clinical research. Her expertise spans oncology, hematology, immunology, psychiatry, infectious diseases, and neurology. This diverse background enables her to effectively manage various clinical trials and contribute valuable insights across multiple therapeutic areas.
Education and Pharmaceutical Sciences Expertise
Ryoko Oka studied at Mukogawa Women's University, where she earned a Bachelor of Pharmacy (B.Pharm.) in Pharmaceutical Sciences from 2004 to 2008. Her academic background lays a strong foundation for her roles in clinical trial management and data management in the pharmaceutical industry.