Teye Adusu

Teye Adusu

Senior Compliance Specialist @ Bristol Myers Squibb

About Teye Adusu

Teye Adusu is a Senior Compliance Specialist at Bristol-Myers Squibb in Princeton, New Jersey, with extensive experience in compliance and quality assurance roles across multiple pharmaceutical companies.

Title and Current Role

Teye Adusu is currently serving as a Senior Compliance Specialist at Bristol-Myers Squibb in Princeton, New Jersey, United States. He has been with the company since June 2016, where he focuses on maintaining compliance standards.

Previous Roles in the Pharmaceutical Industry

Teye Adusu has held numerous positions across various pharmaceutical companies. Notably, he worked as a Senior Study Director at Westat in Cambridge, UK, for five months in 2012-2013. He served as a Medical QAP at Pfizer in Cambridge, UK, from 2010 to 2011. Before that, he was an Associate Director at Ariad Pharmaceuticals, Inc., from 2008 to 2010 and a Senior Manager at Biogen from 2004 to 2008. Early in his career, he worked at Takeda Oncology as a Senior QA Associate from 2002 to 2004 and at Pfizer as a Clinical Research Scientist in Groton, Connecticut, from 1999 to 2000.

Education and Expertise

Teye Adusu boasts a diverse educational background. He studied at Emory University, where he earned a Master of Public Health in 2010. He also holds a Master of Science from the University of Guelph, gained between 1989 and 1992. Additionally, he earned a Doctor of Veterinary Medicine degree from Havana Veterinary College. Adusu also attended Cornell University and Toronto BD Center, adding to his extensive academic qualifications.

Volunteer Work

In 2003, Teye Adusu volunteered at the Global Health Council. This role reflects his commitment to global health initiatives and showcases his willingness to contribute beyond his professional obligations in the pharmaceutical industry.

International Work Experience

Teye Adusu has international work experience, having held positions in both the United States and the United Kingdom. His roles have spanned various responsibilities in compliance, quality assurance, and clinical research, indicating a broad and adaptable skill set suited for the global pharmaceutical landscape.

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