ASSOCIATE DIRECTOR, BIOSTATISTICS

Sun Pharmaceutical Industries
Princeton, NJ, United States
Full-time

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Sun Pharma Vision : Reaching People And Touching Lives Globally As A Leading Provider Of Valued Medicines

Sun Pharmaceutical Industries Ltd. (Sun Pharma) is the fourth largest specialty generic pharmaceutical company in the world with global revenues of over $ 4.

5 billion US Dollars. Supported by more than 40 manufacturing facilities, we provide high-quality, affordable medicines, trusted by healthcare professionals and patients, to more than 100 countries across the globe including the United States.

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Our Global Code of Conduct governs every aspect of our operations. Sun Pharma is a family of thousands of people, working across many countries, speaking multiple languages, and all united, with one common purpose : to make good health accessible and affordable to local communities and society at large.

Through active fieldwork, dedicated research teams, and in recognition of the efforts who work behind the scenes to combat illness and disease, the Sun Pharmaceutical Group helps as many people as possible, to secure their right to good health.

The way we work every day is important to us.

DOWNLOAD OUR CODE OF CONDUCT

Our Global Code of Conduct governs every aspect of our operations. Sun Pharma is a family of thousands of people, working across many countries, speaking multiple languages, and all united, with one common purpose : to make good health accessible and affordable to local communities and society at large.

Through active fieldwork, dedicated research teams, and in recognition of the efforts who work behind the scenes to combat illness and disease, the Sun Pharmaceutical Group helps as many people as possible, to secure their right to good health.

The way we work every day is important to us.

DOWNLOAD OUR CODE OF CONDUCT

SPARC is seeking an Associate Director of Biostatistics to provide support to Phase 1-3 clinical research studies.

The Associate Director will :

  • Serve as the statistical lead on one or more clinical development programs
  • Engage in planning, methodology, and analysis for Phase 1-3 clinical studies, not limited to protocol development, sample size calculation, authoring of statistical analysis plans, data review, analysis implementation and interpretation
  • Review of case report forms (CRFs), data management plans, data specifications and clinical study reports, creation of randomization schedules, provide statistical analysis and reports to Data Monitoring Committees (DMCs)
  • Work with internal staff and / or vendors to assure that all programming and statistical analyses are completed
  • Provide statistical / programming support for responses to regulatory authorities related to submission reviews
  • Statistical programming / analyses including transfer, creation, conversion, and formatting of SAS data
  • Serve as the statistical representative on cross-funcitonal teams
  • Participate in the development and maintenance of SOPs

Requirements :

  • PhD in Statistics required with 4 or more years of related experience or MS in Statistics with 6 or more years of related experience
  • Expert in SAS programming with demonstrated experience using Base SAS, SAS Stat, macros, analyses and reports
  • Very good written and oral communication skills
  • Great collaborator and ability to work with clinical experts
  • Excellent mathematical skills and problem solving skills
  • 30+ days ago
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