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Lead and finalize electronic regulatory document publishing, manage major dossier submissions/amendments, mentor junior staff, support Medical Writing/Biostatistics/Programming/Regulatory teams, and serve as escalation point for technical troubleshooting.

The Principal Biostatistician leads statistical analysis for clinical trials, providing insights and ensuring accurate reporting on trial data.

The Associate Director, Project Management leads global clinical trials, ensuring project delivery on time and within budget while mentoring project teams.

The Principal Clinical Data Manager oversees data management tasks for clinical research projects, ensuring data quality, managing teams, and training data managers.

The Strategic Consultant in Biostatistics drives consulting efforts, client relationships, and provides expertise in clinical trial design and regulatory implications, while mentoring teams and ensuring service solutions.