Qualissima, Spécialiste de la recherche et des essais cliniques

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Who are we ?

Staff

Qualissima associates a great variety of talents: experience, versatility and complementarity insure a full control of our projects.


Olivier BLIN

Olivier BLIN is a University Professor – Hospital Practitioner, Clinical Pharmacologist and neuropsychiatrist. He is in charge of the Center of Clinical Pharmacology and Therapeutic Evaluations at the Assistance-Publique-Hôpitaux of Marseille. He is also responsible for the Team Feelings Pharmacology and Physiopathology within the " Institute of the Cognitive Neurosciences of the Mediterranean , UMR CNRS 6193". Olivier Blin a is member of the American Society for Clinical Pharmacology and Therapeutics and of the American College of Clinical Pharmacology, past-president of the French Association of Biological Psychiatry, Secretary of the Clinical Pharmacology Section of the French Society of Pharmacology and Therapeutics. He is a co-founder of Qualissima and acts as scientific consultant.


Sophie TARDIEU

Sophie TARDIEU is a pharmacist, former Hospital resident and Hospital Practitioner in Public Health. She brings her methodological support in the field of the pharmaco epidemiology and of the medical evaluation. She is a member of the French Society of Pharmacology and Therapeutics. She is a co-founder of QUALISSIMA.


Séverine PITEL

Séverine PITEL owns a PhD in sciences. After a thesis on the clinical development of a therapeutics innovation, she joined QUALISSIMA in November, 2007 as clinical project manager. She ensures clinical studies coordination and performs medical writing. She also participates in the preparation of clinical trial authorization submissions for clinical trials assessing drugs or medical devices.


Romain COMBALAT

Romain COMBALAT owns a Master's degree in Sciences. After the obtention of his Diploma: "Investigators training for clinical trials" (DIU-FIEC), he joined QUALISSIMA in September, 2008 as Clinical Research Associate. He participates in the update of the Standard Operating Procedures, in the organization and the follow-up of clinical trials, and in the preparation of clinical trial authorization submissions.


Aurore DERMY

Aurore DERMY owns a Master's degree in Health Engineering - Clinical evaluation of therapeutic trials. After an experience of clinical research associate in an hospital, she joined the company in April 2010 for an internship and she is now Clinical Reserach Associate.

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