Clinical Specialist III

Job Summary

A company is looking for a Clinical Specialist III to join their team in the Clinical Safety department.

Key Responsibilities

• Manage adverse event processing, including report review and expedited reporting
• Assess processing levels for adverse events and author safety documents and plans
• Conduct Clinical Trial Safety Review meetings and ensure safety event adjudication before data snapshots

Required Qualifications

• Minimum bachelor's degree or equivalent experience in a science-related field
• Minimum 5 years of clinical trial experience in safety
• Proven experience with clinical trial safety
• Medical device background is preferred
• Knowledge of Good Clinical Practice (GCP) and experience with safety event processing