Senior Biostatistician at ProPharma

Location: St. John's

Elevate your expertise at Pro Pharma as a Senior Biostatistician Consultant. Lead statistical analyses and provide insights in clinical trials while collaborating with cross-functional teams in a hybrid work environment.

In this full-time role based in the United States or Canada, you will shape statistical methodologies and ensure the quality of statistical deliverables. The position calls for an individual with deep expertise in clinical trial design, SAS programming, and regulatory frameworks. This role not only enhances your career but also contributes to advancing crucial drug therapies.

Key Responsibilities:

• Lead statistical activities for clinical trials and data analysis

• Develop and review statistical analysis plans and reports

• Provide statistical guidance to clinical operations and regulatory teams

• Maintain SAS programs following good programming practices

• Mentor junior statisticians in statistical methodologies

Requirements:

• Ph.D. or M.S. in Biostatistics

• 3+ years of relevant work experience

• Knowledge of CDISC data structures and clinical design

• Strong interpersonal and project management skills

• Expertise in SAS or R programming

Utilize your biostatistics expertise and project management skills to influence critical clinical initiatives at Pro Pharma.
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