Clinical IT SME: AI-Driven Trials Architect

Infosys Limited; Parsippany-Troy Hills (NJ); Presencial; USD 114.000 - 149.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Long-term Disability

Health reimbursement accounts

401(k) plan

Descripción de la vacante

Infosys Limited in Parsippany, NJ seeks a Domain Consultant 3 to drive business analysis for clinical trial domains and lead IT solution evaluations. You will craft architectures, document systems, and guide integration with existing infrastructure to meet client goals.

The role emphasizes regulatory awareness, data management, and scalable design within life sciences projects. U.S. work authorization is required; some relocation/travel may be needed.

Formación

• End-to-end clinical trial management experience across study start to closeout.
• Experience with clinical data management applications (OC/RDC/TMS).
• Experience with clinical reporting for internal and FDA requirements.
• Experience in Computer Systems Validation activities in life sciences projects.

Responsabilidades

• Perform business analysis on trial processes to identify opportunities and optimize value chains.
• Evaluate IT solutions for alignment with client goals and strategic decisions.
• Create documentation and articulate complex technical concepts for stakeholders.
• Research third-party products and assess features, performance, and integration.
• Create solution architectures and architectural diagrams for scalable systems.
• Lead technical implementation and maintenance strategies for reliability.

Conocimientos

End-to-end Clinical trial management

Clinical data management applications

Clinical reporting (FDA)

Computer Systems Validation

Educación

Bachelor’s degree or foreign equivalent

Descripción del empleo

Infosys Limited in Parsippany, NJ seeks a Domain Consultant 3 to drive business analysis for clinical trial domains and lead IT solution evaluations. You will craft architectures, document systems, and guide integration with existing infrastructure to meet client goals.

The role emphasizes regulatory awareness, data management, and scalable design within life sciences projects. U.S. work authorization is required; some relocation/travel may be needed.