Senior Statistical Analyst

2 days ago

Ahmedabad, Gujarat, India beBeeStatistical Full time ₹ 1,50,00,000 - ₹ 2,00,00,000
Job Summary:

We are seeking an experienced statistical programmer to provide programming support for clinical trials.

Key Responsibilities:
  • Exceed expectations and responsibilities of a senior statistical programmer
  • Implement CDISC and other regulatory standards
  • Develop and maintain internal SAS programming conventions
  • Coordinate and ensure the accuracy and completeness of activities for assigned projects
  • 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; including but not limited to:
  • Analysis datasets (SDTM, ADaM, other derived datasets)
  • Tables, listings and figures
  • xml/Reviewer's Guide
  • Integrated summaries
  • Perform ad hoc analyses of current and legacy databases
  • 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
  • Standard Operating Procedures (SOPs)
  • Strong understanding of departmental and company procedures; ability to guide others on procedures
  • May participate in the development and revision of department SOPs
  • Business Development
  • May support the business development process; RFI completion, proposal development, bid defense participation, attendance at industry/scientific meetings, etc.
Required Skills and Qualifications:
  • The ideal candidate should have 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.)
  • Excellent oral and written communication skills, organizational skills, and attention to detail are required

This is an equal opportunity employer and welcomes diversity in the workplace.

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