Clinical Safety Specialist

Job Summary

A company is looking for a Clinical Safety Specialist to manage safety and complaint data throughout clinical studies.

Key Responsibilities

• Review and assess clinical study Adverse Events (AEs) and device deficiencies
• Interact with investigational sites and clinical monitors to obtain additional information as needed
• Collaborate with Regulatory Affairs and Product Complaint Reporting teams for timely reporting of safety events

Required Qualifications

• Equivalent to a bachelor's degree
• Minimum of 1 year of relevant experience
• Basic medical terminology and interpretation of clinical data
• Proficiency in Microsoft Office (Excel, Word, PowerPoint)
• Fundamental knowledge of Clinical Research