2021 -2021 Director Regulatory Affairs and Pharmacovigilance @
2017 -2021 Director Regulatory Affairs @
2018 -2019 Director Regulatory Affairs, Programme Team Leader @
2016 -2017 Regulatory Lead @
2013 -2016 Senior Regulatory Project Manager @
2009 -2013 Regulatory Affairs Professional @
2002 -2009 Project Manager Drug Regulatory Affairs and Pharmaceutical Development @
2001 -2002 Pharmacist, Regulatory Affairs, Animal Health @
Anne Kirkegaard Education
The University of Bonn
Masters
2004-2006
University of South Australia 2001-2001
Danmarks Farmaceutiske Universitet
Master of Science (Pharmacy)
1995-2001
Université Stendhal (Grenoble III)
(French Language, Social Science)
1994-1995
San Marcos High School 1991-1992
Anne Kirkegaard Skills
Product Development
eCTD
Regulatory Affairs
Pharmaceutical Industry
Analytical Chemistry
Clinical Development
Validation
Sop
GMP
Regulatory Submissions
Drug Development
Pharmacovigilance
GCP
Regulatory Requirements
Anne Kirkegaard Summary
Anne Kirkegaard, based in Copenhagen, DK, is currently a Director, Regulatory Affairs and Medical Writing at Pharma IT. Anne Kirkegaard brings experience from previous roles at FluoGuide A/S, Novozymes, Ros Therapeutics and Cyxone. Anne Kirkegaard holds a 2004 - 2006 Masters @ The University of Bonn. With a robust skill set that includes Product Development, eCTD, Regulatory Affairs, Pharmaceutical Industry, Analytical Chemistry and more. Anne Kirkegaard has 1 emails and 1 mobile phone numbers on RocketReach.
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