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The IMS Specialist I role involves supporting clinical development projects at Syneos Health, collaborating with teams to streamline processes and improve customer satisfaction.

The Sr CRA performs site management, ensures compliance with regulations, verifies data integrity, supports recruitment, and collaborates with project teams.

Manage and coordinate clinical research studies, ensuring compliance with regulations, maintaining study documentation, and facilitating communication among stakeholders.

The R Statistical Programmer develops programming code, ensures quality outputs, collaborates with teams, and manages multiple projects while adhering to regulatory guidelines.

Coordinate safety and pharmacovigilance activities, including data management, cleaning, validation, and adherence to regulatory guidelines.

Conduct monitoring of clinical research, ensure compliance with protocols, develop monitoring tools, and provide training to junior staff.

Conduct monitoring of clinical research studies, ensure compliance with guidelines, develop monitoring plans, and manage project components. Collaborate with teams for successful study conduct.

Lead a team of Azure Data Engineers, develop ETL/ELT solutions using Azure tools, and translate customer needs into technical requirements while ensuring process governance.

Conduct monitoring of clinical research studies, ensure compliance, develop quality monitoring tools, manage lower-level professionals, and collaborate with cross-functional teams.

The Senior QA Tester will design and maintain automation solutions for testing across applications, improving quality and efficiency. Responsibilities include development of automated scripts, CI/CD integration, collaboration for test coverage, and managing documentation.