Clinical Research Associate II/Sr

At Parexel, this role involves identifying and resolving issues that may impact the conduct of clinical trials while ensuring studies are run in line with ICH/GCP and local laws. Monitors investigator sites to ensure data quality and compliance, maintaining accurate site-level information and managing corrective actions with site personnel. The position supports the development of therapies by facilitating efficient study execution and engaging with healthcare professionals to uphold client credibility.