Remote Project Manager: IRT & Study Lifecycle Lead

SSi People; Princeton (NJ); Remote; USD 90,000 - 130,000; Full time

Job summary

SSi People seeks a technically minded Project Manager II to drive end-to-end Interactive Response Technology activities in a remote setting. You will help drive study timelines, system quality, stakeholder readiness, and continuous improvement across the project lifecycle.

The ideal candidate has 3+ years in IRT PM or IRT database design/development, with strong PM capabilities and administrative coordination skills, understanding of the IRT lifecycle within clinical studies.

Qualifications

• 3+ years of Interactive Response Technology project management experience or IRT database design/development experience.
• Combination of IRT/RTSM knowledge with PM skills and strong administrative capabilities.
• Understanding of the IRT lifecycle and clinical study environment.

Responsibilities

• Support IRT development from kickoff through go-live, change control, maintenance, and closeout while helping maintain study timelines.
• Coordinate user acceptance testing with stakeholders and CROs, draft test scenarios and provide execution support.
• Monitor system change requests with clinical teams to define updates and ensure completion through the lifecycle.
• Support vendor performance, data transfer issue resolution, documentation development, process improvement, and stakeholder training materials.

Skills

IRT knowledge

Project management

Administrative skills

Education

Bachelor's degree in biology/life sciences/CS

Job description

SSi People seeks a technically minded Project Manager II to drive end-to-end Interactive Response Technology activities in a remote setting. You will help drive study timelines, system quality, stakeholder readiness, and continuous improvement across the project lifecycle.

The ideal candidate has 3+ years in IRT PM or IRT database design/development, with strong PM capabilities and administrative coordination skills, understanding of the IRT lifecycle within clinical studies.