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Job Description & How to Apply Below
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 strong multitasking skills
Bring your expertise in clinical safety data to Everest and enhance quality in groundbreaking research.
Position Requirements
10+ Years
work experience
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