Senior Safety Monitor

Job Summary

To support the Pharmacovigilance and Medical Monitoring department, the full-time Senior Safety Monitor I will implement safety monitoring activities for clinical projects, supervise Pharmacovigilance-related projects, and ensure compliance with Good Clinical Practice and relevant safety regulations while working remotely.

Key responsibilities

• Perform safety monitoring activities and oversee the collection and reporting of adverse drug reaction cases
• Guarantee compliance with quality standards and maintain accurate reporting to relevant health authorities
• Act as a mentor for junior colleagues and drive corporate activities related to safety training and process improvement

Required qualifications

• Bachelor's Degree in pharmacology, nursing, or a related scientific discipline with relevant clinical experience
• 4-6 years of experience in research or with a pharmaceutical company, focusing on safety monitoring/pharmacovigilance
• 1-3 years of preferred mentoring experience in safety monitoring/pharmacovigilance
• Working knowledge of MedDRA and WHO Drug coding is preferred
• Excellent clinical judgment and ability to communicate complex clinical issues effectively