MAIN TASKS :

Activities must be carried out by adhering to the policies, study protocols, procedures, standard operating procedures, GLP/GCP regulations and regulatory organization standards relative to their division/service and to Anapharm inc.

1.Verifies, using the appropriate method (in-process or other), generated raw data by ensuring the consistency of the sequence of events, when applicable.

2.Verifies the accuracy of raw data included in various tables, when applicable.

3.Ensures, jointly with the personnel in question, that the appropriate answers are received regarding observations and that corrections and documents are followed-up properly.

4.Communicates the necessary information to the people in charge in order to ensure the smooth conduct of the project.

5.Participates, as needed, in the initial and continuous training of new quality control reviewer (clinical).

6.Helps prepare and review documents during regulatory agency visits.

• Education: College diploma in science or another appropriate field.
• Professional experience: 1 - 2 years relevant work experience.
• Computer knowledge: Word, Excel.
• English (level): Must be able to understand simple messages and follow basic instructions.
• Other (optional): Experience in a regulatory context would be considered an asset.