Amsterdam Area, Netherlands
Regulatory Affairs Manager
Pharmaceuticals
Education
Rijksuniversiteit Groningen 1998 — 2005
Master of Science (M.Sc.), Medical Biology
ASG de Friese Wouden
Bogerman college
van Hall Instituut
Experience
RENOLIT Nederland B.V., part of the RENOLIT Group November 2014 - Present
TEVA Pharmachemie January 2013 - November 2014
VSM Geneesmiddelen bv 2011 - March 2012
IATEC BV April 2008 - November 2010
Leiden University Medical Center 2006 - 2008
Skills
Process Improvement, Excel, Life Sciences, SOP, Vaccines, Infectious Diseases, Medical Affairs, Oncology, English, Microsoft Office, GCP, Clinical, Sop, Biotechnology, Molecular Biology, Regulatory Requirements, CRO, EDC, Research, ICH-GCP, CTMS, Regulatory Submissions, Pharmaceuticals, Clinical Trial..., Clinical Trials, Data Management, Clinical Development, GxP, Medical Writing, MedDRA, Pharmacovigilance, Pharmaceutical Industry, Regulatory Affairs, Lifesciences, Drug Development, Pharmaceutics, Analysis, Drug Safety, Clinical Monitoring, Clinical Operations, Immunology, Clinical Research, Validation, Compliance, GMP, Clinical Data Management