Nooshin Zamani, M.Sc.
About Nooshin Zamani, M.Sc.
Nooshin Zamani, M.Sc., is the Manager of Patient Safety at Bristol Myers Squibb in Montreal, Quebec, Canada, with over 10 years of experience in the pharmaceutical industry.
Current Position at Bristol Myers Squibb
As the Manager of Patient Safety at Bristol Myers Squibb, Nooshin Zamani, M.Sc., plays a critical role in ensuring the safety of patients who use the company's products. Located in Montreal, Quebec, Canada, she is responsible for monitoring and managing the safety profiles of pharmaceutical products, ensuring compliance with regulations, and assessing risk factors. Her position involves a comprehensive understanding of patient safety protocols, data management, and regulatory compliance. Her expertise ensures the well-being of patients and the integrity of Bristol Myers Squibb’s product portfolio.
Work Experience at Celgene
Nooshin Zamani worked at Celgene as a Drug Safety Specialist from 2017 to 2020 in the Toronto, Canada Area. During her three years at Celgene, she was involved in pharmacovigilance activities where she monitored, evaluated, and reported adverse drug reactions. Her position demanded a deep understanding of drug safety protocols and regulatory requirements. She contributed significantly to ensuring that the products released into the market were safe for consumption, thereby protecting patient health and meeting regulatory standards.
Professional Background at Bayer HealthCare
Nooshin Zamani held several pivotal roles at Bayer HealthCare in the Toronto, Canada Area and Iran. These roles included Pharmacovigilance Specialist (2013-2016), Drug Safety Associate (2012-2013), and Deputy Medical Advisor and Deputy Local Drug Safety Manager (2008-2010). Her experience at Bayer HealthCare involved comprehensive drug safety and regulatory functions. She was responsible for monitoring pharmacovigilance activities, ensuring compliance with safety guidelines, and providing medical advisory support. Her extensive experience at Bayer HealthCare has equipped her with a robust understanding of global regulatory standards and effective drug safety management.
Education and Certifications
Nooshin Zamani holds a Master of Science in Pharmacology from the University of Ottawa, where she studied in the Cellular and Molecular Medicine Department from 2002 to 2006. She also completed a Post Graduate Certificate in Regulatory Affairs from Humber College, where she studied from 2011 to 2012. Her educational background has provided her with a strong foundation in pharmacology, regulatory affairs, and drug safety. These qualifications have been instrumental in her successful career in the pharmaceutical industry, underpinning her expertise in regulatory guidelines and safety protocols.
Global Experience and Expertise
Nooshin Zamani has over 10 years of experience in the pharmaceutical industry, with more than 2 years of global exposure in Regulatory Affairs, Clinical Trial Management, Pharmacovigilance, and Drug Safety. She possesses significant knowledge of Canadian, US, and EU regulations and guidelines for drug products and medical devices. This global experience has allowed her to develop excellent data management, evaluation, and analytical skills, which are crucial for ensuring compliance and patient safety. Her diverse experience emphasizes her capability to manage complex drug safety and regulatory challenges on an international scale.