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The Site Management Associate I coordinates communication between sites and vendors, manages clinical supplies, ensures compliance with regulations, and supports site training and documentation management.

Lead the implementation of ContractPodAI, integrate AI into legal operations, oversee project management and user adoption, and engage stakeholders.

The Product Manager will lead the implementation of a global CLM system, facilitating stakeholder engagement, overseeing testing, and driving user adoption through change management.

The Associate, Process Improvement will develop and maintain ontologies, collaborate with teams to improve processes, and analyze data to support knowledge management initiatives.

As a Full stack Developer at PSI, you will develop and maintain business applications, process requests, prepare documentation, and conduct testing while adhering to development standards.

The Clinical Research Associate conducts monitoring visits, reviews CRFs, manages site communications, and supports regulatory submissions at PSI.

The Site Management Associate supports clinical research projects by managing data, documentation, and communications among stakeholders, ensuring compliance, and facilitating audits.

The Principal Statistician will lead statistical activities in global clinical trials, conduct analyses, develop protocols, and review deliverables while guiding statisticians and programmers.

The Principal Statistician leads statistical activities in global clinical trials, ensuring integrity and compliance in statistical analyses, protocols, and deliverables, while coordinating with teams and clients.

The Principal Statistician will lead statistical activities for global clinical trials, oversee statistical analysis, and liaise with cross-functional teams on project-related inquiries.