CTI Clinical Trial and Consulting Services seeks a regulatory specialist to advise project teams on country-specific regulatory requirements for clinical studies. You will perform compliance assessments, adapt study documents for each country and site, and submit to IRB/EC/CA as needed.The role requires 3–5 years of pharmaceutical regulatory experience, plus expertise in European trial start-up and CTIS processes. Hybrid work options and career development support are offered.
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📌 European Clinical Trials Regulatory Start-Up Specialist (Hybrid) (España)
🏢 Cti Clinical Trial And Consulting Services
📍 España
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