Provide statistical support to the research and development organization, focusing on clinical
Collaborate with cross-functional teams to design, analyze, and report clinical studies and other
Develop protocols and statistical analysis plans; implement sound statistical methodology for
Identify data collection instruments, report data issues, and prepare datasets with programming
Perform statistical analyses under supervision and ensure high-quality outputs on agreed timelines.

🎯 Requirements

MS (4+ years) or PhD in Statistics, Biostatistics, or related field.
Ability to perform statistical computations and simulations.
Experience with pharma clinical trials (internship or employment).
Strong technical competence and excellent oral and written communication.

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