1. Nathalie Langevin
Date of birth: 14th January 1979
nathalie.langevin@gbmail.com
06.21.55.66.77
75 rue des Martyrs, 75009 Paris
Professional objective
With 4 years of professional experience as a clinical research associate and 1 year of professional experience as a
study start-up specialist, I have proven organisational and project development skills. My principal
objective is to obtain a post as a project manager in clinical research.
Work experience
2009 to present Clinical Research Associate, RPS Research France
In charge of a phase II study (4 sites) and 2 phase III studies (12 sites) in oncology/haematology:
-Pre-trial, initiation, monitoring and close-out visits ; monitoring visits with CRA trainees
-Preparation of regulatory documents (informed consent, synopsis, etc.)
-Participation in financial contract preparation with sites
-Training of site staff in protocol and good clinical practices
-Follow-up of study timelines and site budgets
-Oversight of procedures and of good clinical practices
-Management and archiving of study documents
Education
2009 Clinical research associate training at Supsanté Paris
2004 PhD specialised in organic chemistry at the University Paris-XI
2000 Postgraduate certificate in chemistry at the University of Nantes
1999 Master’s Degree in chemistry at the University of Nantes
Other skills
Technical Good command of common software (Office), Medidata Rave and Phase Forward
Languages Good command of English; working knowledge of German and Spanish
Hobbies
Running, fitness, traveling