Parmiss Keyhani
About Parmiss Keyhani
Parmiss Keyhani is a Senior Clinical Research Associate at Bristol Myers Squibb in Queensland, Australia, with over 18 years of experience in the clinical trials industry.
Current Role at Bristol Myers Squibb
Parmiss Keyhani currently holds the position of Senior Clinical Research Associate at Bristol Myers Squibb. She has been with the company in this role since May 2016, working out of Queensland, Australia. In this capacity, she leverages her extensive background in clinical trials and site monitoring to manage and oversee clinical studies.
Previous Roles at Bristol Myers Squibb
Before her current role, Parmiss Keyhani has had a long history with Bristol Myers Squibb. She worked as a Study Start Up Specialist from 2015 to 2017 in Queensland, Australia. Additionally, she served as a Senior/Clinical Site Monitor from 2003 to 2011 in Sydney, New South Wales, Australia. Throughout her tenure at the company, Parmiss has accumulated a wealth of experience in clinical site monitoring and study start-up roles.
Experience at Parexel
Parmiss Keyhani worked at Parexel as a Clinical Trials Specialist focused on Study Start Up for one year from 2012 to 2013 in Queensland, Australia. This role allowed her to further hone her skills in clinical trials and study start-up processes.
Educational Background
Parmiss Keyhani studied at the University of New South Wales (UNSW) where she achieved a Master of Drug Development from 2000 to 2003. Prior to this, she earned a Bachelor of Science in Immunology, completing her studies in 1992. Her education laid a strong foundation for her career in clinical research and drug development.
Career Beginnings at Serono Pharma
Parmiss Keyhani began her career in the clinical research industry at Serono Pharma, where she worked as a Clinical Research Associate from 2001 to 2003 in Sydney, New South Wales, Australia. This initial role provided valuable experience that would shape her long and successful career in clinical trials.