Clinical Research Associate

Company Description

Zenovel specializes in delivering high-impact solutions across Good Clinical Practice (GCP), Good Manufacturing Practice (GMP), and Regulatory Affairs in the pharmaceutical and biotech industries. With over 20 years of global experience, we assist companies in ensuring their trials, facilities, and products meet international regulatory standards efficiently. Our services span a wide range, including clinical development support, manufacturing compliance, and strategic regulatory guidance with expertise across diverse study designs and therapeutic areas. Committed to compliance-driven growth, Zenovel transforms complex regulations into competitive advantages for our partners. Our mission is to enable scalable, secure, and globally compliant solutions.

Role Description

• Take part in monitoring plan meeting

• Overseeing the progress of a BA/BE studies or clinical trial, and of ensuring ...

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Submit your application today and join our talented team at ZENOVEL.