Job highlights
. Robust proficiency implementing the latest CDISC SDTM / ADaM standards
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
. Solid SAS data manipulation,analysis and reporting skills- with strong output programming experience

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.
Solid 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.

📌 Principal Programmer Noida (India)
🏢 Medtek Dot Ai
📍 India