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We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.

As part of our global FSP team, you will perform and coordinate all aspects of clinical monitoring and site management activities in close collaboration with the sponsor. As a Clinical Research Associate (Level II), you will conduct both on-site and remote monitoring visits to ensure protocol and regulatory compliance, as well as proper documentation.

Acting as a site management specialist, you will ensure that clinical trials are conducted in accordance with the approved protocol, ICH‑GCP guidelines, applicable local regulations, and SOPs. You will play a key role in ensuring subject...