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The Specialist coordinates user access and management for clinical systems, monitors compliance, supports onboarding/offboarding, and collaborates with stakeholders to ensure study readiness and system functionality.

As a Specialist in Regulatory Operations, oversee compliance and regulatory activities for clinical trials, particularly for U.S. sites, ensuring adherence to FDA and global standards. Support IRB submissions and maintain essential regulatory documentation.

The Specialist, Regulatory Operations oversees regulatory activities for clinical trials, ensuring compliance and supporting site operations. Responsibilities include managing IRB submissions, regulatory documentation, and collaborating with cross-functional teams.

The Senior HR Business Partner will align business strategy with people plans, oversee talent management, ensure compliance in HR practices, and mentor junior HR staff.

The Senior Software Engineer will develop full-stack applications using TypeScript, collaborate with designers, implement APIs, and ensure code quality in a remote setting.

The Senior Data Engineer will design, develop, and maintain data pipelines, optimize data performance, and collaborate with stakeholders to deliver effective data solutions.

The Principal Investigator oversees clinical trials, ensuring protocol adherence and patient safety while managing study staff and participating in regulatory compliance activities.

As Provider Partnerships Program Manager, you will manage project structures, analyze data, and enhance provider collaboration to support clinical studies.

The Mobile Site Vehicle Specialist role focuses on supporting mobile clinical trial operations through logistics management, inventory handling, and technical troubleshooting, while providing field support for research activities.

The Operational Compliance Specialist ensures compliance in clinical trials, manages CAPA processes, and improves operational quality and efficiency across the region.