Service de pharmacologie médicale
- Clinical Research Associate
2015 - 2017
Realizing setting-up meetings of studies
Planning site visits : contact, request for files, schedule appointments with doctors
National business travel : 3 or 4 days a week:
Updating of Investigator file and checking of consent forms
Data collection in oncology (1 year and a half), data quality-control,
Monitoring of datas collected by doctors: solving correction requests
Writing visits reports
Completing the monitoring database to facilitate the conduct of studies
Writing standard operating procedures
Telephone questionnaires with patients
Management of Pharmacovigilance circuit
