Senior Manager Biostatistician Consultant US
ClinChoiceUnited Statesfull-time
AI Summary: Design statistical analyses and write statistical analysis plans for clinical drug trials across multiple therapeutic areas, collaborating with study teams and regulatory submissions. Work involves protocol design, data analysis, and reporting to regulatory agencies rather than software development.
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Originally posted onremoteok on 5/15/2026
Full Description
Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says itâs the best of both worldsâ¦.
ClinChoice is searching for an Senior Manager Biostatistician Consultant to join one of our clients.
ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the clientâs counterparts.
Job Duties
This position is responsible for working with study team members and the project statistician to contribute to design of early/late-stage protocols across multiple therapeutic areas, help draft protocols or amendments, develop and write statistical analysis plans, and perform statistical analyses for interim and final reports to be submitted to regulatory agencies.
ClinChoice is searching for an Senior Manager Biostatistician Consultant to join one of our clients.
ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the clientâs counterparts.
Job Duties
This position is responsible for working with study team members and the project statistician to contribute to design of early/late-stage protocols across multiple therapeutic areas, help draft protocols or amendments, develop and write statistical analysis plans, and perform statistical analyses for interim and final reports to be submitted to regulatory agencies.
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