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Principal Programmer

1 month ago

Nagar, India Medtek.AI Full time

Why Choose Us ? We have talented professional staff experts in clinical research, medical writing, IT services, data science, and software development. Our professionals are experts in keeping your priorities and goals to follow updated business trends. Our expertise drives cost efficiency to our client. We are flexible, innovative, reliable, and passionate. Let's collaborate We are extremely honoured and grateful to have such talented people in our team. Their selfless efforts and dedication towards giving out our clients with the best of their capabilities made us a renowned and reputed incorporation today. We are a forward-looking organization and are motivated by the trust and confidence that our mutually beneficial relationship with our customers will take them and us to unattained heights of the universe.

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.