A leading clinical contract research organization is seeking a Regulatory Submissions Coordinator in Madrid. This key role involves preparing and filing clinical trial applications, ensuring compliance with regulations, and advising on regulatory requirements. Candidates should have a Bachelor’s degree in Life Sciences, experience in regulatory documentation, and be fluent in both Spanish and English. The position offers a versátil work environment and competitive compensation along with numerous professional growth opportunities.br#J-18808-Ljbffr
📌 Madrid Regulatory Submissions Coordinator – Study Start-Up
🏢 Medpace
📍 Madrid
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