Clinical Safety Specialist

Job Summary

A company is looking for a Clinical Safety Specialist to ensure accurate safety assessments of adverse events in clinical studies.

Key Responsibilities

• Interact with clinical sites and field monitors to verify source data for safety event adjudication
• Review and code adverse events and serious adverse events using MedDRA, ensuring accuracy across studies
• Collaborate with internal and external teams to develop and execute clinical safety plans and ensure compliance with reporting standards

Required Qualifications

• Bachelor's degree
• Minimum 2 years of experience in clinical research
• Proficient with electronic databases used for clinical trials
• Experience with Good Clinical Practices (GCP)
• Bachelor's degree in life science is preferred