Eligibility:
- PhD or MS in statistics or related discipline with 7-9 years of relevant experience.
Key Responsibilities:
- Provide broad statistical support, including trial design, protocol, and CRF development on specific studies.
- Provide statistical input into Data Monitoring Committee (DMC) activities, including development of DMC charters and analysis plans.
- Lead production and quality control of randomization, analysis plan, statistical reports, statistical sections of integrated clinical reports, and other supporting documents.
- Perform sample size calculations, generate randomization lists, and write statistical methodology sections for inclusion in study protocols.
- Serve as a non-voting independent statistician, providing data and analysis for DMC review.
Job Location:
- Hybrid
Application Process:
- Interested candidates can WhatsApp their resume to 9215590007.
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