What are the responsibilities and job description for the Senior Programmer position at cGxPServe?
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 post-submission activities.
- Ensure programming outputs align with industry standards and project expectations.
- Maintain up-to-date documentation for all study-related 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.
- Bachelor's 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 problem-solving abilities.
- Excellent oral and written communication skills for cross-functional collaboration.
- Detail-oriented, dependable, and self-motivated.
