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A Range of Possibilities

Senior Biostatistician

date posted 02/18/2021
contract type Full time
job id R2586870
location Hyderabad, India

Mission statements

  • The Senior Biostatistician will work with Medical Affairs biostatisticians and MedHub biostatistics and programming personnel to implement statistical analysis plans and provide QC’d data packages including tables, figures, and listings for use in publications (i.e. abstracts, posters, oral, presentations, and manuscripts)
  • The Senior Biostatistician will ensure SOPs are followed and timelines and quality metrics are met

Collaboration

  • Local biostatistics and programming teams
  • Global Medical Affairs biostatisticians
  • Global Medical Affairs Scientific Communications personnel

Duties & Responsibilities

People

  • Develop and maintain effective relationships and collaborations with the end stakeholders (Medical community) and local biostatistics and programming team members within the allocated Global business unit and product – with an objective to develop statistical data outputs.

Performance/Process

  • Conduct appropriate post-hoc statistical analyses of clinical trial data
  • Design, develop, test, implement, and document statistical programming in high-level software packages e.g. SAS
  • Produce well documented data packages that include tables, listings, and figures
  • Work closely with the Lead Biostatistician and Lead Programmer to develop and implement project QC plans and timelines.
  • Review appropriate biomedical and clinical research literature related to assigned project(s)

Customer

  • Work closely with Global Medical Affairs biostatisticians to identify statistical analysis needs and assist in developing assigned deliverables

Knowledge, Skills & Competencies / Language

  • Stakeholder management
  • Project management
  • Ability to work independently and within a team environment
  • Advanced knowledge of SAS statistical procedures
  • Excellent English language knowledge – written and spoken

Qualifications

  • Master's degree/Ph.D. in biostatistics or statistics or epidemiology and 2-4 years (Ph.D.)/6-8 years (M.Sc.) of experience required

Requirements of the job

  • Pharmaceutical/healthcare industry exposure
  • High proficiency in statistical methods used in the pharmaceutical industry
  • Advanced SAS and other statistical computing software skills in a clinical data environment across multiple therapeutic areas
  • Expertise in the use of data management applications and database/file structures, specifically with respect to CDISC requirements
  • Autonomy in the management of activities; ability to manage multiple conflicting high priority deadlines
  • Capacity to respond to unscheduled changes in project workload

At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers. We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all.

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