Our Bay Area pharmaceutical client is recruiting for a Clinical Data Associate to join their growing team

Summary:

• Assist in implementing routine activities involving CDM interaction with other study management team members
• Review study protocols and assist site coordinators, investigators, and field clinical staff in collecting routine data to meet the protocol requirements in a timely manner
• Demonstrate ability to identify problems early and communicate escalation issues appropriately
• Ensure completeness, accuracy and consistency of routine clinical data and data structure
• Utilizes routine reports to track study progress and ensure timeliness and quality expectations are met

Requirements:

• Bachelor's degree in Life Science with 3 plus years of biopharmaceutical experience
• Knowledge of FDA/EMA regulations, support of needs for NDA and other regulatory submissions, and familiarity with web-based Electronic Data Capture (EDC) and clinical data management systems
• Demonstrate understanding of project timelines and metrics to ensure databases are delivered to set timelines

**Local Candidates Only**