Upsilon Global
The CRO is seeking a Cape Town-based Medical Monitor to provide medical and safety oversight throughout the study. While the role is expected to be predominantly remote, occasional on-site support may be required depending on study needs.
Key Responsibilities:
• Medical oversight of the study and participating sites
• SAE review and safety assessment
• Ongoing medical support to investigators and study teams
• Participation in study-related meetings and safety discussions
• Oversight of medical coding activities
• Review of study documents, including the Protocol and Investigator's Brochure
• Participation in occasional pre-study meetings ahead of first patient enrolment
Qualifications & Experience:
• Medical Doctor (MD/MBChB) qualification
• Active HPCSA registration required throughout the engagement
• Previous Medical Monitoring experience within clinical trials
• Strong safety review and pharmacovigilance experience
• Experience in neonatal clinical research strongly preferred
• Experience in NICU-based studies highly desirable
• Previous First-in-Human and/or Phase I study experience preferred
No skills specified