Clinical Specialist III
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
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
