22 sep
|
Cti Clinical Trial And Consulting Services
|
Madrid
22 sep
Cti Clinical Trial And Consulting Services
Madrid
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.
📌 European Clinical Trials Regulatory Start-Up Specialist (Madrid)
🏢 Cti Clinical Trial And Consulting Services
📍 Madrid