Drive success in clinical trials with Everest Clinical Research as a Clinical Safety Data Associate. Work in a flexible setting from home in Canada or at our Markham office, focusing on critical safety data review tasks. As a Clinical Safety Data Associate, you will play a pivotal role ensuring the integrity and quality of safety data across various trials.

This position demands a background in medical information management and the ability to collaborate effectively with multiple stakeholders. Candidates should possess a strong understanding of data coding and clinical trial processes. Key Responsibilities:

- Coordinate development of safety data review protocols
- Conduct thorough reviews of clinical safety data
- Assist Clinical Data Managers in data handling
- Provide coding support using established dictionaries
- Engage with teams to resolve data discrepancies Requirements:
- Relevant degree (RN, M.D., Pharm.D., etc.)
- 2-3 years’ clinical data management experience
- Knowledge of safety data coding and analysis
- Effective communication at all levels
- Well-organized with solid multitasking skills Bring your expertise in clinical safety data to Everest and enhance quality in groundbreaking research.

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