Senior Programmer
Senior Programmer
Posted on :
15-04-2025
Employer Active
1 Vacancy
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Job Description
Responsibilities:
- Develop and perform SAS programming for data processing and analysis.
- Collaborate with statisticians and other programmers to ensure accuracy consistency and adherence to quality control (QC) procedures.
- Support study deliverables and manage timelines for statistical data analysis and reporting.
- Document and track programming differences between developers and Statistical QC programmers.
- Provide programming support for ISS/Client and postsubmission activities.
- Ensure programming outputs align with industry standards and project expectations.
- Maintain uptodate documentation for all studyrelated programming tasks.
- Develop program test and maintain validation/edit checks in SAS.
- Perform peer programming validation to ensure quality and consistency.
- Offer technical expertise and support to the Data Management team.
- Participate in study setup database lock activities and team meetings.
- Manage project priorities and timelines efficiently.
- Apply knowledge of statistical terminology clinical data structures regulatory standards and protocol designs.
- Bachelors degree in Biostatistics Mathematics Computer Science or a relevant scientific discipline.
- 5 years of SAS programming experience in the pharmaceutical biotech or CRO industry (Oncology experience preferred).
- Strong SAS programming macro development and SAS graphing skills.
- Experience with CDISC standards (CDASH/SDTM/ADaM).
- Familiarity with ISS (Integrated Summary of Safety) and Client (Integrated Summary of Efficacy) is a plus.
- SAS Certification (Base Programmer for SAS 9 or Advanced Programmer for SAS 9 preferred.
- Strong analytical and problemsolving abilities.
- Excellent oral and written communication skills for crossfunctional collaboration.
- Detailoriented dependable and selfmotivated.
Employment Type
Full Time
Key Skills
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