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As a Statistical Programmer I at Parexel, you will support clinical trial development by utilizing statistical programming to analyze data and contribute to project success.

Lead enterprise-wide AI adoption by translating technical AI concepts for non-technical stakeholders, curating education and communications, partnering with change management and L&D, triaging requests, and building a team to drive measurable AI adoption across the organization.

The Senior Regulatory Affairs Associate monitors and analyzes regulatory changes, translating them into actionable insights, supports strategic decision-making, and engages in industry networking.

The Clinical Research Associate II is responsible for maintaining study integrity and compliance, managing site relationships, resolving site issues, and ensuring timely completion of project goals in line with clinical trial protocols.

The role involves developing regulatory strategies, managing PMDA consultations, and leading regulatory submissions related to clinical development for pharmaceutical companies in Japan.

The Senior CRA ensures quality site management and monitoring of clinical trials, addressing protocol-related issues while maintaining compliance and investigator relations.

Supports biomarker data science workflows by running, maintaining, and improving R-based analysis pipelines, packages, templates, and flow cytometry gating workflows. Manages data intake, harmonization, documentation, quality control, reproducibility, and deliverable tracking. Contributes to Git-based development and reusable Claude Code libraries, including standards for testing, documentation, and AI-assisted coding. Collaborates with scientists and operational teams on clinical and molecular data analyses.

As a Clinical Research Associate at Parexel, you will participate in clinical trials and contribute to regulatory processes, ensuring optimal health outcomes.

The Regulatory Affairs Consultant will manage the labeling lifecycle, ensure compliance with regulations, prepare documents for submissions, and support labeling initiatives in a global team.

The Senior / Principal Statistical Programmer leads statistical programming for clinical trials, providing expertise and monitoring quality, timelines, and resource allocation while mentoring a global team.