Join Everest Clinical Research as a Clinical Safety Data Associate, focusing on safety data management. Enjoy adaptable remote work opportunities or take part in our on-site team in Toronto, Ontario. This role is designed for a meticulous professional with a background in clinical trial data management.

As a Clinical Safety Data Associate, you will be responsible for reviewing, coding, and managing safety data throughout the clinical trial process. Your expertise will ensure high-quality data and compliance with industry standards. Key Responsibilities:

- Develop and maintain safety data review plans
- Review laboratory and safety data while documenting findings
- Collaborate with Clinical Data Managers for data accuracy
- Provide medical insights for SAE and coding activities
- Assess and confirm laboratory normal ranges and units Requirements:
- Degree in Pharmacology or health-related sciences
- 2-3 years in clinical trial data management
- Familiarity with safety data coding practices
- Strong communication and organizational skills
- Independent with project management abilities Be part of Everest's success in clinical research—support safety data processes with precision and excellence.

📌 Everest Safety Data Associate Remote (Markham)
🏢 Everest Clinical Research Services
📍 Markham