Paris Area, France
Global Clinical Operations Inspection readiness, eClinical/EDC/CTMS, NonClinical/Clinical Submission Readiness
Pharmaceuticals
Education
Université Paris Descartes 1994 — 1995
DESS (MSc), Drug Metabolism, Pharrmacokinetics and Toxicology
Université Denis Diderot (Paris VII) 1990 — 1993
Master, Biochemistry and Pharmacology
Experience
PointCross Life Sciences September 2012 - Present
Wyeth Research now Pfizer PGRD January 2009 - July 2012
Wyeth Research January 2007 - December 2008
Wyeth Research January 2001 - December 2006
Wyeth-Ayerst Research October 1997 - December 2000
Skills
Infectious Diseases, Pharmaceutical Industry, Clinical Monitoring, Regulatory Submissions, Pharmacovigilance, CRO, Validation, Cardiology, FDA, Quality Assurance, Vaccines, GxP, Clinical Development, Pharmaceuticals, Clinical Data Management, Clinical Research, R&D, Neurology, Clinical Operations, Business Process, Regulatory Affairs, Clinical Trial..., EDC, Computer System..., Quality Control, Biotechnology, Sop, CTMS, Project Management, Oncology, Key Performance..., Therapeutic Areas, GMP, GCP, Drug Development, Biopharmaceuticals, Business Intelligence, Lifesciences, Drug Discovery, 21 CFR Part 11, Clinical Trials