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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

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Cv natalie langevin

  • 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