Statistical Programmer

1 - 6 years

1 - 6 Lacs

Posted:1 week ago| Platform: Foundit logo

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Work Mode

On-site

Job Type

Full Time

Job Description

Mission statements

  • The Statistical Programmer 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 Statistical Programmer will develop, implement, and document non-routine macros and advanced techniques
  • The Statistical Programmer will ensure SOPs are followed and timelines and quality 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
  • Closely follow QC plans and timelines set by senior members of the MedHub biostatistics and programming team
  • Remain current on advanced programming methods

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
  • Ability to manage timelines
  • Ability to work independently and within a team environment
  • Advanced SAS programming skills
  • Excellent English language knowledge - written and spoken

Qualifications

  • Bachelor or Master of Science degree or equivalent in Statistics, Computer Science, Mathematics, Engineering, Life Science, or related field
  • Masters degree 1-2 years/B.Sc. 3-6 years of relevant experience required

Requirements of the job

  • 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

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Sanofi

Pharmaceutical Manufacturing

Paris France

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