Lead and provide statistical support for clinical studies.
Act as the lead statistician on assigned studies, overseeing statistical strategy and deliverables.
Author and review key statistical documents (SAPs, ADS, clinical study reports).
Collaborate with cross-functional teams including Clinical, Programming, Data Management, and
Communicate statistical concepts and results clearly to technical and non-technical stakeholders.
Provide guidance to statistical programmers as needed and ensure adherence to regulatory standards.

🎯 Requirements

MS or PhD in Statistics, Biostatistics, or a related field.
Experience in Pharmaceutical/CRO environments with clinical trials; interaction with regulators
Strong oral and written communication skills; able to explain complex stats to diverse audiences.
Demonstrated understanding of the drug development process and regulatory requirements (FDA, ICH

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