03 ago
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Medpace
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Madrid
A leading clinical contract research organization is seeking a Regulatory Submissions Coordinator in Madrid.
Por favor, verifique que tiene el nivel de experiencia y las cualificaciones adecuadas leyendo la descripción completa de esta oportunidad a continuación.
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. xhfqzwm
The position offers a adaptable work environment and competitive compensation along with numerous professional growth opportunities.
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📌 Madrid Regulatory Submissions Coordinator – Study Start-Up
🏢 Medpace
📍 Madrid