Paris
I am currently occupying a position of Clinical Trial Specialist at the CRO PAREXEL International. This position implements itself in the Study Start Up unit and thereby concerns all the criticial steps to obtaining an SIV (Site Initiation Visit) ready status for sites in France.
My numerous scientific background and past professional experiences have allowed me to develop communication skills and thus to work efficiently as a team member. I have also had the opportunity to acquire leadership qualities, strong management and organisational skills, and the capacity to immediately adapt to new environments which allows me to be quickly independent and operational. All of these qualities are essential to perform efficiently as a Clinical Trial Specialist in the innovative and rapidly evolving field that is clinical research and development of new drugs.
While in this position, I was able to participate in the proper conduct of clinical studies in compliance with GCP and regulations to ensure that the development of new drugs is carried out with respect to patient safety. I have had numerous tasks and was involved in Ethics Committee preparation and submissions as well as Feasability studies.
Mes compétences :
Good communication skills
Good organisational skills
Rigourous
Scientific curiosity and quickly independant
Flexible and good adaptability
Anticipation and takes initiatives
