BENGALURU · FULLTIME
Principal Statistical Programmer
EMMES Services
Bengaluru · onsite · Posted 4d ago
Sourced from
Undisclosed7–9 yrsfulltimeBengaluru
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Section · 01
About this role
Job Summary
Responsibilities
Qualifications
Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.
The Principal Statistical Programmer is a senior-level contributor responsible for designing, developing, validating, and maintaining statistical programming deliverables to support clinical trials and regulatory submissions. This individual serves as a technical expert on study and project teams, providing leadership in the application of statistical programming standards and regulatory guidance (e.g., CDISC, ICH, FDA).
Responsibilities
- Lead the development, validation, and maintenance of SDTM and ADaM datasets and associated documentation.
- Program complex Tables, Listings, and Figures (TLFs) for study reports, publications, and submissions.
- Review and interpret statistical analysis plans (SAPs) to ensure accurate implementation in code.
- Serve as lead programmer on multiple studies and/or projects, coordinating efforts across internal teams and CROs.
- Provide technical oversight and mentoring to junior programmers and contractors.
- Collaborate closely with Biostatistics, Data Management, and Clinical teams to deliver timely and accurate outputs.
- Ensure programming deliverables comply with industry standards (CDISC, FDA, EMA) and internal SOPs.
- Contribute to the development and implementation of programming standards and reusable code libraries.
- Participate in quality control, peer review, and validation of programming deliverables.
- Prepare and review submission ready datasets, define.xml files, and reviewer guides for regulatory authorities (e.g., FDA, EMA).
- Support integrated summaries of safety (ISS) and efficacy (ISE) analyses for NDA/BLA/MAA submissions.
- Use tools such as Pinnacle 21, OpenCDISC, and define.xml generators to ensure submission compliance.
- Performs other duties as assigned.
- Complies with all policies and standards.
Qualifications
- Bachelors Degree or Masters degree in Computer Science, Statistics, Mathematics, Life Sciences, or related field.
- 7-9 years in statistical programming within the pharmaceutical, biotech, or CRO industry.
- Expert level proficiency in SAS Base, SAS Macro, and SAS SQL.
- In depth experience with CDISC SDTM and ADaM standards.
- Proven track record of supporting clinical trial reporting and regulatory submissions.
- Strong understanding of ICH GCP, 21 CFR Part 11, and FDA and EMA regulatory expectations.
- Excellent problem solving skills and attention to detail.
- Strong communication and collaboration skills.
Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.
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Section · 02
Skills
CfrBIOTECHNeuroscienceadamclinical researchclinical trialsCROmathematicsgoogle cloud platformProgrammingProgrammerGeneratorsOphthalmologyCdiscHealthcareData ManagementmaintenancecomplianceNDAPharmaceuticalLife SciencesArtificial Intelligence
Section · Company
About EMMES Services
EMMES Services
25
employees
Bangalore / Bengaluru, Karnataka
India
₹12.1L PA avg
Avg at EMMES Services
About
EMMES SERVICES
Industries
BiopharmaBiotechnologyClinical TrialsHealth CareMedical
Employee ratings
10 reviews
3.1/ 5
Culture
3.8
Career growth
3.2
Work-life
4.1
Employees rate it well for
Compensation & Benefits34Work-Life Balance32
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