Regulatory Affairs Associate

Job Summary

A company is looking for a Regulatory Affairs Associate responsible for preparing and submitting clinical trial applications.

Key Responsibilities

• Prepare, review, and submit clinical trial applications to Health Canada's Directorates
• Act as the company's contact and regulatory liaison with Health Canada
• Maintain a database for regulatory submissions and ensure compliance with regulatory requirements

Required Qualifications

• Bachelor's degree in Life Sciences
• Understanding of clinical research and drug development processes
• Familiarity with applicable regulatory guidelines
• Good computer skills (Microsoft Word, Excel, PowerPoint)
• Professional attitude and ability to work in a multi-disciplinary team