2014 -2018 Senior Director, QPPV, Head of QPPV Office @
2013 -2014 Director, QPPV, Head of Global Pharmacovigilance Support @
2013 -2014 Director, Head of Safety Operations and Risk Management @
2012 -2013 Director, European Head of Global Standards and Compliance @
2010 -2012 Director, Drug safety Relations and Compliance, International Drug Safety @
2008 -2010 Director, Drug Safety in LOCs, International Drug Safety @
2006 -2008 International Clinical Project Manager @
2002 -2006 Safety Data Manager @ Nycomed
Berit Andersen Education
Københavns Universitet
Master of Industrial Drug Development (MIND) (Pharmaceutical Sciences)
2006-2013
Ringsted Nursing School
Bachelor (Registered Nurse)
1988-1991
Berit Andersen Skills
Pharmaceutical Industry
Pharmacovigilance
GCP
CRO
Drug Safety
Clinical Development
Clinical Trials
Sop
EDC
Medical Writing
ICH-GCP
Clinical Monitoring
Regulatory Requirements
Medical Affairs
Regulatory Submissions
Clinical Research
Drug Development
Regulatory Affairs
CTMS
Therapeutic Areas
Oncology
Clinical Data Management
21 CFR Part 11
Risk Management
People Development
People Skills
Organizational Leadership
Organizational Design
Project Management
Leadership
Ich Gcp
Strategic Planning
Support
Strategy
Microsoft Excel
Change Management
Management
Organizational
Berit Andersen Summary
Berit Andersen, based in Denmark, is currently a Safety Director at LINK Medical Research. Berit Andersen brings experience from previous roles at Lundbeck, LEO Pharma and Genmab. Berit Andersen holds a 2006 - 2013 Master of Industrial Drug Development (MIND) in Pharmaceutical Sciences @ Københavns Universitet. With a robust skill set that includes Pharmaceutical Industry, Pharmacovigilance, GCP, CRO, Drug Safety and more. Berit Andersen has 2 emails and 2 mobile phone numbers on RocketReach.
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