Megan Whitnall
About Megan Whitnall
Megan Whitnall is a Clinical Operations Manager at BeiGene in Sydney, Australia, and an Associate Clinical Project Manager at Novotech.
Title: Clinical Operations Manager
Megan Whitnall holds the title of Clinical Operations Manager. In this role, she oversees clinical operations and ensures adherence to regulatory and ethical standards. Her responsibilities include managing clinical trials, coordinating with research teams, and ensuring the successful execution of clinical projects.
Company: BeiGene
Since January 2019, Megan Whitnall has been working at BeiGene in Sydney, New South Wales, Australia. Her current role is Clinical Operations Manager. BeiGene is a global biopharmaceutical company focused on developing molecularly targeted and immuno-oncology drug candidates for the treatment of cancer.
Company: Novotech
Megan Whitnall also serves as an Associate Clinical Project Manager at Novotech. Novotech is a clinical CRO (Contract Research Organization) that provides clinical development services across the Asia-Pacific region. In her role, Megan is responsible for managing clinical research projects and coordination among clinical sites.
Education and Expertise: University of Sydney
Megan Whitnall completed her doctoral studies at the University of Sydney. She achieved a Doctor of Philosophy degree, focusing on her research from 2000 to 2003 and again from 2006 to 2011. Her advanced education in this prestigious institution underpins her expertise in clinical research and operations.
Previous Experience: Clinical Research and Project Management
Megan Whitnall has extensive experience in clinical research and project management. She has worked at Novotech in various roles, including Senior Clinical Research Associate and Clinical Research Associate III. Her prior positions include Clinical Research Associate II at IQVIA, outsourced to Roche, and Clinical Research Associate at Inventiv Health Clinical, also outsourced to Roche. Megan started her career at Roche as a Clinical Trial Assistant and later as a Clinical Trial Monitor.