Medical Safety Monitor

We are seeking a Medical-Safety Monitor to provide medical safety oversight for clinical trials. In this role, you will act as the main medical safety contact for study teams, ensuring subject safety medical data integrity. You will work closely with cross-functional teams under the supervision of the Medical Director, Safety & Pharmacovigilance.

If you’re passionate about advancing patient safety in clinical research, we’d love to hear from you.

Key Responsibilities

• Serve as the medical safety expert for assigned trials
• Review and assess safety data (e.g adverse events, serious adverse events, labs, ECGs, vitals)
• Participate in Safety Review Meetings & be responsible for DMC interactions
• Support safety signal detection and risk assessment
• Provide medical input to study documents and clinical data review
• Collaborate with Clinical Operations, Biostatistics, Regulatory & PharmacovigilanceV teams

Qualifications

• MD degree
• 4+ years’ experience in clinical research / medical or safety roles
• Excellent communication skills in English

Preferred

• Experience in pharmacovigilance and safety evaluation
• Experience in clinical data interpretation