Utrecht Area, Netherlands
Clinical Data Standards Manager at GSK
Pharmaceuticals
Education
Wageningen University 2001 — 2009
Master's degree, Cell/Cellular and Molecular Biology
Experience
GSK March 2015 - Present
Novartis Vaccines August 2014 - February 2015
Merck Sharp & Dohme May 2012 - July 2014
Genzyme Europe BV May 2011 - May 2012
Kendle International July 2009 - May 2011
Kendle International December 2008 - June 2009
Skills
Project Management, Clinical Trial..., Data Analysis, CTMS, Clinical Data Management, Data Entry, Process Improvement, Study Design, Data Management, Protocol Development, Change Management, SAS/SQL, CRF design, Immunology, CRO, Data Validation, Excel, Programming, Clinical Research, Phase II, Clinical Monitoring, Biotechnology, MedDRA, Clinical Trials, ICH-GCP, GCP, Inform, Phase I, FDA, Creativity, Data Modeling, Phase III, Validation, 21 CFR Part 11, CDISC, Neurology, SPSS, EDC, Pharmaceuticals, Clinical Development, Quality Assurance, Databases, Research Project..., SOP, Word, Phase Forward Inform, Life Sciences, Healthcare, Clinical, Pharmacokinetics