Statistical Programmer

17 hours ago

Pune, Maharashtra, India beBeeStatistical Full time ₹ 1,04,000 - ₹ 1,30,878
Statistical Programmer Job Description

 

  •  
  • Job Summary: 
  • A statistical programmer is required to work on clinical trials, including SDTM and ADaM datasets, tables, listings, and figures. 
  • The successful candidate will be responsible for end-to-end statistical programming, collaborating with biostatisticians, sponsors, and project teams. 

 

  •  
  • Responsibilities: 
  • Develop custom programming code using SAS or other software to generate summary tables, listings, graphs, and derived datasets. 
  • Ensure outputs meet quality standards and project requirements. 
  • Perform validation programming and collaborate with other programmers and biostatisticians to resolve discrepancies. 
  • Maintain organized, complete, and up-to-date project documentation, testing, and verification/quality control programs. 
  • Manage multiple projects, set priorities, and adapt daily workload according to project timelines. 
  • Develop specifications for datasets and outputs of varying complexity according to statistical and sponsor requirements. 
  • Anticipate and address potential programming issues to establish efficient programming practices. 
  • Prepare and contribute in internal meetings, sponsor meetings, kickoff meetings, and bid defense meetings. 
  • Act as lead statistical programmer, directing programming activities of other personnel and monitoring progress on deliverables. 
  • Review project documentation such as SAPs, mock shells, programming specifications, annotated CRFs, and SAS database designs. 
  • Provide feedback to project team members to reduce inefficiencies and improve programming quality. 
  • Mentor programming personnel, develop training materials, and guide new associates in programming processes. 
  • Transfer deliverables and perform other work-related duties as assigned. 
  • Minimal travel may be required.
Required Skills and Qualifications
  •  
  • 5+ years of experience in Clinical Statistical Programming. 
  • Expertise in end-to-end programming, including SDTM, ADaM, and TLFs. 
  • Undergraduate degree in a scientific or statistical discipline, or equivalent combination of education and demonstrated programming experience. 
  • Extensive programming experience in SAS or other required software, preferably in a clinical trial environment. 
  • Excellent written and verbal communication skills; ability to read, write, speak, and understand English.

We offer competitive compensation and benefits package.

Key qualifications include 5+ years of experience in clinical statistical programming, expertise in end-to-end programming, and excellent communication skills.

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