Statistical Science Associate Director

Vizen Life Sciences Pvt Ltd; Hyderabad; On-site; INR 1,800,000 - 3,000,000; Full time

Job summary

Vizen Life Sciences Pvt Ltd in Hyderabad, India, invites a Senior Statistician to lead statistical analysis for pharmaceutical development. You will design studies, run simulations, interpret results, and guide CRO partners to ensure quality and timeliness.

The ideal candidate holds MSc/PhD in Statistics or Biostatistics with 5+ years in pharma data analysis, programming in R or SAS, and experience in Phase III oncology study design and execution.

Qualifications

• MSc/PhD in Statistics, Biostatistics, or recognised equivalent to stats MSc.
• 5+ yrs of experience in pharmaceutical development, data analysis and interpretation; preferably Phase III Oncology study design.
• Strong knowledge of programming in R and/or SAS.
• Experienced in conducting simulations.

Responsibilities

• Analyze, interpret, summarize and present results of clinical study.
• Conduct statistical modelling to predict the timing of interim and final event-driven analyses in a clinical study.
• Direct project work, including statistical staff and/or CRO partners, to ensure delivery to standards, quality and time.
• Develop study design options and provide high quality decision support to enable the business to make informed decisions about a study or project.
• Investigate and apply novel statistical approaches, for relevant statistical issues and/or regulatory guidance and/or value demonstration, including modelling and simulation.
• Mentor/coach and support the training of statistics staff.

Skills

R programming

SAS programming

Education

MSc/PhD in Statistics or Biostatistics

Job description

Responsibilities

• Analyze, interpret, summarize and present results of clinical study
• Conduct statistical modelling to predict the timing of interim and final event-driven analyses in a clinical study
• Direct project work, including statistical staff and/or CRO partners, to ensure delivery to standards, quality and time
• Develop study design options and provide high quality decision support to enable the business to make informed decisions about a study or project
• Investigate and apply novel statistical approaches, for relevant statistical issues and/or regulatory guidance and/or value demonstration, including modelling and simulation
• Mentor/coach and support the training of statistics staff

Qualification & Expeirence

• MSc/PhD in Statistics, Biostatistics, or recognised equivalent to stats MSc
• 5+ yrs of experience of pharmaceutical development, data analysis and interpretation and experience of program design; preferably, experienced in designing and executing a Phase III Oncology study
• Strong knowledge of programming in R and/or SAS
• Experienced in conducting simulations