Medical Officer

Job Summary

To support clinical trial initiatives, the full-time Medical Officer will manage medical monitoring, provide safety oversight, and engage in protocol development while working remotely.

Key responsibilities

• Lead clinical trial monitoring of safety and efficacy data, ensuring compliance with relevant SOPs and study documents
• Evaluate and assess safety events and protocol deviations throughout the lifecycle of clinical studies
• Collaborate with project teams to develop safety management plans and provide medical input for protocol and study documentation

Required qualifications

• Medical Doctor (MD), MBBS, MBBCh, or equivalent degree
• Minimum of 2 years of experience in clinical practice and pharmaceutical medicine
• Demonstrated expertise in safety and medical monitoring, including serious adverse event reporting
• Experience with regulatory submissions and clinical trial data collection
• Fluency in English with excellent communication skills