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The Manager of CTM will oversee clinical trial operations, ensuring compliance with GCP and regulatory standards while managing cross-functional teams and project outcomes.

The Senior GCP QA Manager leads cross-functional teams to manage Quality Events by conducting RCA and CAPA, ensuring compliance, and liaising with clinical functions and external parties to uphold quality standards.

As a Proposals Writer II, you will develop client-ready proposals, collaborate with experts, and manage project timelines in clinical research.

As a Senior Statistical Programmer I, you will develop and validate SAS programs for clinical trial data analysis, collaborate with biostatisticians, and ensure compliance for high-quality results and reporting.

The Manager, Clinical Systems will oversee the implementation and optimization of clinical systems, ensuring compliance and data integrity while leading a team and collaborating with cross-functional teams.

The role involves providing DMPK expertise, conducting reviews of nonclinical programs, preparing regulatory submissions, and engaging in business development initiatives.