Training "Clinical Research Secretaries and Assistants"

• A day to discover clinical trials, the guidelines for clinical research, and to understand the traceability principles for study documents

Program

• Clinical studies: goals, main steps, organization
• Guidelines: Law related to Public Health Policy and the French Good Clinical Practices
• Study documents: implementation of their control
• The study file: implementation and management

Teaching methods

• A training that balances presentations, games, quizzes, and case studies

Attendees' profile

• Secretaries and Assistants of a Clinical Research Department or of a Clinical Operations Unit

Trainers

• Mrs. Frédérique ALBOUY-NAVARRO (Doctor of Pharmacy)
• Mrs. Catherine MERAT (Doctor of Pharmacy)
• Mrs. Estelle ZERBIB (Doctor of Pharmacy)
• Mrs. Mélanie GENTRIC-GUERIN (Doctor of Pharmacy)

Practical criteria

• Place: Paris area
• Duration: 1 day
• Schedules: 9h30-18h00
• Rate: €800 per attendee (taxes not included), including educational fees, documentation, lunch, and coffee breaks

• Register