ICON plc in the UK or South Africa seeks a Medical Coder to encode adverse events and medical history using MedDRA and WHOdrug. You will deliver scientific operations work to a high standard and collaborate with your team and stakeholders.
The role requires a health-related degree or equivalent experience, 2+ years in pharmacovigilance or clinical data management, and working knowledge of medical terminology and coding. Strong attention to detail and communication are essential.
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Medical Coder: MedDRA & SAE Data Specialist employer: ICON Clinical Research
At ICON plc, we pride ourselves on being a world-leading healthcare intelligence and clinical research organization that champions innovation and excellence. As a Senior Director in Regulatory Affairs, you will thrive in our inclusive culture that prioritises employee growth and well-being, offering competitive benefits such as flexible leave, comprehensive health insurance, and a supportive work-life balance. Join us in shaping the future of clinical development while enjoying a dynamic environment that fosters collaboration and professional development.
