Senior Biostatistician

2 weeks ago


Palakkad, Kerala, India beBeeProgrammer Full time ₹ 15,00,000 - ₹ 25,00,000
Statistical Programming Role

The position of Senior Statistical Programmer is available within a clinical development organization. This role will involve providing programming support for clinical trials, ensuring accurate and high-quality statistical outputs.

This includes programming support for analysis datasets, tables, listings and figures, xml/Reviewer's Guide, integrated summaries, and ad hoc analyses of current and legacy databases.

Responsibilities
  • Programming lead on assigned studies
  • Coordinate and ensure the accuracy and completeness of activities for assigned support programmers.
  • Create and maintain project timelines
  • Support the development of tools and macros to improve quality and efficiency of processes
  • Prepare programming specifications for SDTM, ADaM and other derived datasets
  • Apply knowledge of SAS programming to program/develop and/or validate statistical outputs according to the statistical analysis plan and other specifications;
  • Review and provide input on case report form design
  • Serve as a mentor to other programmers
  • Maintain awareness of scope of work to actual work, alerting management of potential change orders or resourcing needs
  • Work effectively with other programmers, statisticians, data managers, database programmers and other cross-functional team members to ensure accurate and high-quality statistical outputs
Additional Responsibilities
  • May assist in the preparation and review of monthly financial reporting
  • May promote visibility outside of the functional area and effectively interact cross-functionally and in industry
  • May participate in candidate interviews
Requirements
  • A degree in Statistics, Computer Science, or a closely related field; work experience may be substituted for degree
  • Minimum of 4 years direct SAS programming experience in pharmaceutical development or CRO environment
  • Good knowledge of medical terminology and conduct and analysis of clinical trials
  • Knowledge of relevant industry data standards (e.g. CDISC SDTM, ADaM, etc.)

We are seeking individuals from diverse backgrounds and cultures to join our team. Our company values diversity and inclusion, recognizing that it enhances our efficiency and effectiveness.

We are an equal opportunities employer and do not discriminate against any individual based on sex, race, color, age, national origin, religion, gender, gender identity or expression, sexual orientation or sexual preference, pregnancy or maternity, genetic information, marital status, physical or mental disability, medical condition, military or veteran status, or any other basis protected by applicable federal, state, or local law.



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