Biostatistician

Requisition Id:  8050

Key Responsibilities

  • Design statistical analysis plans for clinical trials, observational studies, and laboratory experiments.

  • Perform statistical analyses using appropriate software (e.g., SAS, R, Python).

  • Collaborate with clinical researchers, data managers, and regulatory teams to ensure data integrity and compliance.

  • Interpret and communicate statistical results clearly to cross-functional teams and stakeholders.

  • Prepare tables, listings, and figures for clinical study reports and publications.

  • Support the preparation of documents for regulatory submissions (e.g., FDA, EMA).

  • Stay current with advancements in biostatistics and relevant regulatory guidelines.

  • Contribute to protocol development, data monitoring, and interim analysis.

  • Provide statistical consulting to internal teams on study design and methodology.