Principal Programmer

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PRINCIPAL PROGRAMMER

**Key Responsibilities**:

- Hands on programming role, supporting deliverables in the study/project/portfolio/standards team, of medium or high complex statistical programming deliverables.
- Strong SAS data manipulation, analysis and reporting skills
- with strong output programming experience.
- Strong proficiency implementing the latest CDISC SDTM / ADaM standards.
- Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials’ data.
- Development and execution of statistical analysis and reporting deliverables (e.g safety and efficacy analysis datasets, tables, listings, figures).
- Expertise in the design, development and quality control process for SAS programs used to access, extract, transform, review, analyze and submit clinical data for all requested analyses.
- Provide technical guidance to other statistical programmers, and ensure training and development of team members.
- Lead and manage the programming activities for clinical trials, including development of programming plans, specifications, and programming datasets.

**Qualification;**
- Bachelor or Master (preferred) Degree in Statistics, Mathematics, Bio informatics and Computer Science.
- Minimum 8 years relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency.
- In-depth knowledge of clinical trial design, statistical analysis, and regulatory guidelines.