CLINICAL RESEARCH

                       TO FIT YOURS NEEDS            

    

Senior Clinical Research Independent
Consultant in Clinical Research in France and Europe

 

 

   Ø Stong experience of monitoring in clinical research phases I to IV

  

         o   Phase I : collaboration with CROs Aster (Paris), Biotrial (Rennes and Paris)

                        and LCG Bioscience (Cambridge) ;

                        bioavailibility and pharmacokinetics trials

         o   Phase II : monocentric and multicentric efficacy trials

         o   Phase III : many national and international trials in replacement hormonal therapy, 

                           contraception, infectiology, rheumatology…

         o   Phase IV : implementation and follow-up of questionnaires ; respect of the medical

                          reps' Charter for epidemiologic studies

   Ø Selection, initiation, implementation of trials in investigation centres 

       (private offices and hospital services)

   Ø Investigators meetings for pre-study and study visit

   Ø Trial Master Files updating, in prevision of site's audits

   Ø Privileged contact with investigatorsgood relationship

 

   Services offered to conduct your studies in clinical research

   Ø Procedures in clinical research
   Ø Clinical trial coordination              
   Ø Training in clinical research
   Ø Regulatory submission of clinical trial

 

 

Freelance cra - Senior CRAMonitoring in clinical research - Clinical trial coordination - Regulatory submission of clinical trial - Writing and implementation of procedures in clinical research - Training in clinical research - clinical research associate - clinical research indenpendent - Clinical Research Independent - Senior Clinical Research - links

Monitoring in Clinical Research