RWE & Peri​/Post Approval Statistics Lead

• Manage day-to-day biostatistics activities, supporting your team to deliver quality outcomes.

• Leading a team of statistical analysts and programmers to design and conduct statistical analyses for peri/post approval studies.

• Collaborating closely with cross-functional teams to develop statistical analysis plans and interpret study results.

• Providing statistical expertise and guidance on study design, protocol development, and data interpretation.

• Overseeing the development and validation of statistical models and methodologies for analyzing clinical trial data.

• Contributing to the strategic planning and implementation of statistical analysis projects to support business objectives.

Requirements

• Master’s degree in statistics, computer science, mathematics, or a related discipline
• Minimum of 7 years of experience in statistical analysis within the pharmaceutical, biotechnology, or CRO industry.
• Strong proficiency in statistical software such as SAS, R, or Python.
• Expert knowledge of real world research and peri/post approval designs , statistical methodologies, and regulatory requirements
• Excellent leadership, communication, and interpersonal skills.

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Hard Skills

• statistical analysis
• statistical methodologies
• statistical models
• data interpretation
• study design
• protocol development
• statistical analysis plans
• clinical trial data
• real world research
• programming

Soft Skills

• leadership
• communication
• interpersonal skills