Clinical Project Associate (Quebec City)

Job Summary

We are currently looking for two (2) skilled and motivated Clinical Project Associates to join our growing team. The Clinical Project Associate at ethica CRO Inc. actively assists the clinical team in the planning, implementation, and reporting of clinical studies.

Responsibilities

• Provide support to Clinical Project Managers (CPM) and Clinical Research Associates (CRA)
• Identify, track, and ensure timely delivery of key clinical study milestones
• Assist with the set‑up and maintenance of the Trial Master File (TMF) and the Clinical Trial Management System (CTMS)
• Assist with identifying investigative sites, maintain the site database, and ensure timely updating of site and vendor contact information
• Assist with IRB submissions and communications
• Create confirmation and follow‑up letters for sites
• Assist in the creation and preparation of study documentation and forms
• Assist with...