Key Responsibilities:

• Supporting statistical programming activities for clinical development projects.
• Performing data manipulation, analysis, and reporting of clinical trial data, both safety, and efficacy, utilizing SAS programming.
• Ability to work in cross-functional, multi-cultural and international clinical trial teams.

Qualification:

• Bachelor/ Master in Statistics, Maths, Computer Science.
• Experience in SAS/R/Python/Tableau/Oracle DB.
• Very Strong programming background.
• Excellent analytical & troubleshooting skills.

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.

Key Responsibilities:

• 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)
• Develop and review SAS programs for data analysis, tables, figures, and listings, and ensure accuracy and consistency of data output

Qualifications:

• Bachelor’s or Master’s degree in a data science field, e.g., statistics, mathematics, computer science, bioinformatics,
• Minimum 4 years of SAS programming experience supporting clinical trials in the Pharmaceutical & Biotech industry.
• Strong expertise in SAS programming, and proficiency in other statistical software such as R and Python
• Onsite in Noida , Uttar Pradesh