CTI is seeking a Regulatory Affairs Support specialist to assist in Study Start-Up activities for Clinical Trials and Real-World Evidence projects. You will interact with Ethics Committees, Competent Authorities, and the CTI Legal team to ensure compliant submissions and timely approvals.
You will coordinate site budgets and contract translations, maintain internal systems, and support cross-functional project teams in a fast-paced, integral environment with hybrid work options.
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📌 Country Study Start-Up Specialist (Madrid)
🏢 Cti
📍 Madrid