Jurgen Lissens
clinical project delivery operations risk head of compliance team and business leadership innovation@ Bristol Myers Squibb
Brussels, Brussels Hoofdstedelijk Gewest, Belgium
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Jurgen Lissens is an experienced professional with 23 years of work experience in the pharmaceutical industry. He has expertise in 21 CFR Part 11, biopharmaceuticals, cardiology, clinical development, cro, ctms, biotechnology, and clinical data management. Currently, he holds the position of Associate Director Protocol Management at Bristol-Myers Squibb in Brussels, Belgium. Throughout his career, Jurgen has held various roles in renowned companies such as Smith+Nephew, IQVIA, and IQVIA. He has a strong background in clinical project delivery operations, risk management, and team leadership.
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@bms.com
@msn.com
+1 800332****
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About

Jurgen Lissens. Associate Director Protocol Management at Bristol-Myers Squibb. Location: Brussels Area, Belgium; Industry: Pharmaceuticals...

Work Experience

3401 Princeton Pike, Lawrence Township, NJ, 08648, US

Pharmaceutical Manufacturing

37514
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Jurgen Lissens's Professional Milestones

  • Global Clinical Protocol Manager (2005-03-01~2007-12-01): Implementing a global clinical protocols to improve patient outcomes and optimize clinical process performance.
  • European Clinical Study COOrdinator (2001-01-01~2005-01-01): Coordinated and implemented innovative clinical trials in the European population.
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Education

Ghent University
Ghent University

Biomedical/medical Engineering

1998-2000
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