Prudence Dwyer

Prudence Dwyer

Senior Clinical Research Associate @ BeiGene

About Prudence Dwyer

Prudence Dwyer is a Senior Clinical Research Associate at BeiGene in Australia with over 8 years of experience in clinical research and pharmaceutical medicine.

Current Role at BeiGene

Prudence Dwyer is currently a Senior Clinical Research Associate at BeiGene in Australia. She joined BeiGene in January 2021. In her role, she manages clinical trial sites, ensuring adherence to regulatory requirements and Good Clinical Practice (GCP) guidelines. With over 8 years of experience in clinical research, she brings extensive knowledge in drug development and trial management.

Previous Experience at Syneos Health

Before joining BeiGene, Prudence worked at Syneos Health as a Clinical Research Associate II. During her tenure from 2018 to 2020, she was involved in multiple clinical trials across various phases, contributing significantly to the research and development activities in Sydney, Australia.

Career at PRA Health Sciences

Prudence Dwyer held multiple roles at PRA Health Sciences over different periods. She initially worked as an In-house Clinical Research Associate for 7 months from 2015 to 2016, then transitioned to a Clinical Research Associate role from 2016 to 2017. During her tenure, she contributed to the development and implementation of clinical trial protocols in Sydney, Australia.

Education and Academic Background

Prudence Dwyer holds a Master's degree in Pharmaceutical Medicine from UNSW Australia, which she completed between 2015 and 2018. She also earned a Bachelor's degree in Biomedical Science from the University of Newcastle, finishing her studies in 2014. Her academic background has provided a strong foundation in drug development and clinical research.

Early Career and The AIM Centre

Prudence began her career in clinical research at The AIM Centre as a Clinical Research Administration Assistant in 2015. Over the course of 9 months in Merewether, NSW, she participated in the coordination and administration of clinical trials. This role offered her valuable initial exposure to the field of clinical research.

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