Senior/Principal Statistical Programmer
19 hours ago
Position :
Principal SAS Programmer
Location :
Bangalore/Hyderabad/India
Job Summary
Veramed is seeking a hands-on Principal SAS Programmer with a strong work ethic and attention to detail to join our statistical and programming team. The ideal candidate will provide high-quality programming support for a variety of clinical trials, working on datasets, TFLs, and specifications. This role offers significant exposure to diverse clients and provides a clear opportunity for career growth towards a Lead Programmer or technical specialist position.
Key Responsibilities
- Clinical Programming & Quality Control : Program and perform quality control (QC) on clinical trial datasets and TFLs (Tables, Figures, Listings) in accordance with study specifications and good programming practices.
- CDISC Standards Implementation : Develop and maintain dataset specifications that conform to CDISC (Clinical Data Interchange Standards Consortium) data standards, specifically SDTM and ADaM.
- Mentorship & Leadership : Provide support and mentorship to less experienced members of the programming team, contributing programming expertise and wider industry knowledge as required.
- Collaboration & Communication : Communicate directly with other study team members and client key contacts. You will share updates on ongoing work in internal and client meetings to ensure high-quality, on-time delivery.
- Innovation : Contribute to the development of innovative solutions to aid in study reporting and other programming initiatives.
Required Skills & Qualifications
- A strong background in clinical trial programming, with experience appropriate for a principal-level role.
- Proficiency in SAS programming is a must.
- A deep understanding of the clinical drug development process and relevant disease areas.
- A good understanding of CDISC data standards, including both SDTM and ADaM.
- Awareness of industry and project standards as well as ICH (International Council for Harmonisation) guidelines.
- Strong self-management skills with the ability to work independently, manage competing deliverables, and focus on results.
Preferred Skills
- Experience with other statistical software, such as R.
- Familiarity with various therapeutic areas and different phases of clinical trials.
- Experience presenting at conferences or publishing in professional journals.
- A background in developing innovative solutions or automation for study reporting.
- Knowledge of SAS Macros and other advanced SAS programming techniques.
- Relevant certifications, such as SAS Certified Advanced Programmer.
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