As the Director of Clinical Research at ethica CRO, Tamara’s duties include managing all aspects of the clinical trials, as well as providing support and direction to the clinical project management team.

Tamara joined ethica in 2005 as a Clinical Research Associate where she played an instrumental role in study initiation and site monitoring of Phase I to IV clinical studies throughout Canada and the United States. Over the past fifteen years, the clients of ethica have benefited from Tamara’s exemplary knowledge and expertise in clinical research management and monitoring, her solid work ethics, as well as her outstanding professionalism.

Tamara holds a Master’s Degree of Science in pharmaceutical science from Université de Montréal, a graduate certificate in human resources management from HEC and a BSc in biology from Université de Montréal.