BANGKOK
Clinical trials
• Methodology of a clinical trial (endpoint/criterion, trial design, population analized, statistics, data management..).
• Phase I, II and III trials.
• Phase IV trials (drug monitoring/drug safety, pharmacoepidemiology, risks for the pregnant women, drug dependence).
• Clinical trials in neuro-psychiatry, infectiology, cancerology and cardiology.
Basis of pharmacokinétic and pharmacodynamic
• Absorption, distribution, metabolization, excretion.
• Pharmacokinetic/pharmacodnynamic relation.
• Non linear pharmacokinetic.
• Bioequivalence.
Regulatory aspects and projects
• Regulation and ethic.
• Heatlh autorities and national and international procedures registrations.
• Institutional research.
• Role of the investigator.
• Set up a protocol for a clinical trial.
• Carry out a data collection (CRF).
Computer knowledge
• Bureautique: Word, Excel, PowerPoint.
Languages
• French: mother tongue.
• English : Fluent (Toeic score: 955)
• Spanish: written, spoken and read.
• Creole: mother tongue
• Thai: fluent in speaking , good abilities in reading and writing
Other efficiency
• Good capacity of adaptation and communication.
Mes compétences :
Attaché de recherche clinique
Clinical Research
Clinical Research Associate
Drug safety
Industrie pharmaceutique
monitoring
Pharmacovigilance
Recherche
Recherche clinique
Research
Safety
