ICON Clinical Research is seeking a Senior Medical Writer to lead medical writing strategies for clinical projects. You will own regulatory documents, contribute to protocol and CSR development, and mentor junior writers while coordinating with study teams to meet timelines. The role requires strong regulatory expertise, high-quality writing, and collaboration across cross-functional teams to ensure submission readiness and regulatory compliance in a sponsor-dedicated environment. #J-18808-Ljbffr
📌 Senior Medical Writer: Regulatory Docs (Palma)
🏢 Icon Clinical Research
📍 Palma
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