Hamish Ross
About Hamish Ross
Hamish Ross is the Associate Director of Regulatory Affairs at BeiGene in Sydney, Australia, with extensive experience in regulatory affairs and clinical writing.
Company
Hamish Ross is currently employed at BeiGene, a biotechnology company specializing in molecularly targeted and immune-oncology treatments. He holds the position of Associate Director Regulatory Affairs and is based in Sydney, Australia.
Title
Hamish Ross serves as the Associate Director Regulatory Affairs at BeiGene. In this role, he oversees regulatory activities, ensuring compliance with local and international regulations.
Education and Expertise
Hamish Ross holds a BSc (Hons) in Pharmacology from the University of Otago and a PhD in Neuroscience from the University of Sydney. He has extensive experience in the preparation and compilation of regulatory documents for European and global projects, covering a wide range of therapeutic areas and pharmaceutical forms.
Previous Roles at Merck
Hamish Ross has held various roles at Merck over an eight-year period. He served as a Regulatory Affairs Manager from 2015 to 2019, a Senior Regulatory Affairs Associate from 2014 to 2015, and a Regulatory Affairs Associate from 2011 to 2013. These roles were all based in Sydney, Australia.
Background in Clinical Writing
Before his tenure at Merck, Hamish Ross worked at Catalent Pharma Solutions in Swindon, United Kingdom. He was a Senior Clinical Writer in 2011 and a Clinical Writer from 2009 to 2011. His responsibilities included the preparation of clinical documentation and support for new staff members.