Statistical Programmer I
Advanced Clinical · Ahmedabad · onsite · Posted 21d ago
Undisclosed1–6 yrsfulltimeSourced from
About a minute. You'll make an account on the way through.
About this role
The Statistical Programmer I is responsible for providing programming support for clinical trials.
Responsibilities:
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- Understand and implement CDISC and other regulatory standards
- Follow internal SAS programming conventions
- Apply knowledge of SAS programming to program and/or validate statistical outputs according to the statistical analysis plan and other specifications; including but not limited to:
- SDTM, ADaM or other derived datasets
- Tables, listings and figures
- Review and provide input on case report form design
- May draft programming specifications
- 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
- Additional Responsibilities
- Perform other duties as requested by management
Qualifications:
- The ideal candidate should have a degree in Statistics, Computer Science, or a closely related field or equivalent of education and experience.
- At least 1 year of direct SAS programming experience in pharmaceutical development or CRO environment preferred, but not required.
- Excellent oral and written communication skills, organizational skills, and attention to detail are required
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.
Sourced from naukri
Skills
adamclinical trialsCROSAS ProgrammingstatisticsProgrammingstatistical analysisSdtmProgrammerCdiscSASCommunication SkillsPharmaceutical