Elevate your career with Everest Clinical Research as a Clinical Safety Data Associate. This role allows flexibility with remote work options across Canada while ensuring accurate safety data management for clinical trials. As a Clinical Safety Data Associate, you will play a crucial role in maintaining the quality of clinical trial data.

You will implement and conduct safety data reviews, collaborate closely with Project and Clinical Data Managers, and provide essential medical coding support. Your expertise will contribute significantly to ensuring that all safety data is accurately captured and analyzed. Key Responsibilities:

- Develop safety data review plans for clinical studies
- Review safety data including AEs, SAEs, and lab results
- Coordinate with Project Managers for high-quality data
- Provide medical advice for SAE reconciliation
- Perform coding of AEs using MedDRA Requirements:
- RN, M.D., or Ph.D. in relevant fields
- 2-3 years of clinical trial data management experience
- Knowledge of clinical trial safety coding
- Solid communication and organizational skills
- Ability to manage multiple projects effectively Be a key player in enhancing patient safety and data integrity in clinical research with Everest.

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