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The Clinical Scientist contributes to protocol design, scale management, and provides training on clinical scales while ensuring data consistency and performing statistical analysis.

The Principal Biostatistician oversees statistical tasks, mentors staff, prepares analyses, and ensures high-quality deliverables throughout project lifecycle.

Conduct on-site and remote monitoring of clinical research studies, ensure compliance with protocols, manage junior staff, and prepare reports for regulatory submissions.

The On-site Monitor will manage site activities, ensure compliance with regulations and guidelines, support data collection, and maintain communication with site staff and the project team.

The Sr-Principal Biostatistician will oversee biostatistics personnel, ensure quality project outputs, prepare statistical plans, and contribute to regulatory meetings.

The Principal Biostatistician leads biomarker analysis for clinical studies, develops evaluation plans, conducts data analyses, mentors staff, and ensures accurate statistical deliverables while collaborating across teams.