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The CRA performs clinical monitoring and site management, ensuring compliance with protocols and regulations. Responsibilities include monitoring sites, documenting observations, and managing relationships with investigators.

Supports project team in clinical trials by providing administrative and technical support, managing site activation, and contributing to feasibility assessments while maintaining audit readiness.

Lead all data management activities for clinical studies, mentoring junior staff, maintaining documentation, and ensuring compliance with protocols and regulatory guidelines.

As the Principal Medical Writer, you will produce high-quality medical writing, mentor writers, ensure compliance, and manage complex writing projects.

The Associate Manager Safety Data and PV Systems manages GPS Safety Data operations, supports Oracle Argus Safety system, collaborates with teams, and ensures compliance with regulatory standards.

As a Senior Clinical Data Associate, you will manage data for projects, ensuring accuracy and compliance with protocols, while training junior staff and improving processes.

The Senior Clinical Data Associate supports data management projects, ensuring accuracy, compliance, and improvement of processes while mentoring junior staff.

The Sr Clinical Data Associate manages data for clinical trials, ensures data quality, trains junior staff, and improves data processes.

The Sr Programmer Analyst oversees application configuration and maintenance of Oracle Argus, providing technical solutions and ensuring compliance with industry standards through collaboration with business users and project teams.

The Associate Finance Systems Analyst supports and enhances Finance Information Systems with a focus on Oracle Cloud EPM, improving operations through system analysis, support, and project management.