Elevate your career with Everest Clinical Research as a Clinical Safety Data Associate. Contribute to safety data review for clinical trials in a dynamic and supportive environment, either on-site in Toronto or remotely across Canada. Everest is looking for a detail-oriented Clinical Safety Data Associate.

In this key position, you will ensure high-quality safety data management while collaborating closely with Project Managers and Clinical Data Managers. Ideal candidates will possess robust organizational skills and a broad knowledge base in clinical trial safety data coding and management. Key Responsibilities:

- Develop standard safety data review plans and checklists
- Perform safety data review, identifying and resolving issues




- Coordinate high-quality data collection with project teams
- Provide medical advice during SAE reconciliations
- Conduct coding using MedDRA and WHODrug dictionaries Requirements:
- RN, M.D., M.Sc., or Ph.D. in relevant fields
- 2-3 years’ experience in clinical trial data management
- Strong knowledge in safety data management
- Exceptional oral and written communication skills
- Ability to manage multiple projects effectively Join Everest and play a crucial role in managing clinical safety data with a focus on quality and collaboration.

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