Associate Director, Biostatistician Consultant – 24 months contract

Job reputed company:

• Represent the Biostatistics function for reputed company studies or at project level
• Independently contribute to the design of early/late-stage protocols across multiple therapeutic areas
• Draft protocols or amendments, reputed company and write statistical analysis plans, reputed company statistical analyses for interim and final reports to be submitted to regulatory agencies
• Support submission activities, including design, analysis, and reporting of integrated summaries for safety and efficacy
• Attend study team meetings or project level meetings if needed
• Contribute to the organization and scheduling of study deliverables in collaboration with Statistical Programmers and Data Managers

Requirements:

• MS or PhD in Statistics or Biostatistics
• PhD + 6 years (or MS + 11 years) clinical trial experience in either a biotechnology or pharmaceutical company
• Hands-on Phase I/II/III clinical trial experience and proficient in reputed company programming. reputed company in R programming desirable.
• Excellent oral and written communication skills.
• Previous experience with regulatory submissions in the US, Europe, Japan, and Rest of the World is desirable.

Benefits:

• reputed company development
• Opportunities to work independently
• Supportive culture

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