Experienced SAS Programmer (Navi Mumbai)

Medpace Clinical Research India; Navi Mumbai; On-site; INR 1,000,000 - 1,500,000; Full time

Benefits offered by this job

Flexible work environment

Competitive compensation and benefits package

Structured career paths

Job summary

Medpace Clinical Research India is seeking a Senior SAS Programmer to join our Biostatistics team in Navi Mumbai. This full-time, office-based role involves leading projects, writing SAS programs for data analysis, and ensuring data quality and compliance.

The ideal candidate will have a Bachelor/Master’s degree in a relevant field and at least 5 years of SAS experience. We offer a flexible work environment and a competitive compensation package with opportunities for professional growth.

Qualifications

• 5+ years' experience with SAS.
• Excellent knowledge of CDISC standards.
• SAS Certification.

Responsibilities

• Propose and develop specifications for new projects.
• Write SAS programs for analysis datasets, tables, listings, and figures.
• Program edit checks for external data.

Skills

SAS programming

CDISC standards

Analytical skills

Communication skills

Education

Bachelor/Master’s Degree in relevant field

Tools

SAS

Job description

Senior SAS Programmer

Our corporate activities are growing rapidly, and we are currently seeking full-time, office-based Senior SAS Programmers to join our Biostatistics team in India, Mumbai. This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.

Overview

Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 6,000 people across 40+ countries.

Responsibilities

• Propose and develop specifications for new projects and serve as a project team leader
• Write SAS programs for use in creating analysis datasets, tables, listings, and figures
• Using SAS, program, validate and maintain mapped database
• Program edit checks for external data
• Responsible for the setup, validation and maintenance of mapped databases, integration of external data with associated edit checks, writing programs independently with good quality for use in creating analysis datasets, tables, listings, and figures.
• Responsible for mapped database setup, validation and maintenance, and external data integration & edit checks, validation, and maintenance

Qualifications

• Bachelor / Master’s Degree in math, Statistics, health informatics, data science, computer science, or life sciences field
• 5+ years' eperience with SAS
• Excellent knowledge of CDISC standards
• SAS Certification
• Thorough understanding of the pharmaceutical industry and Federal Regulations regarding electronic records
• Excellent analytical, written and oral communication skills
• Good English written/communication skills is required

Benefits

• Flexible work environment
• Competitive compensation and benefits package
• Competitive PTO packages
• Structured career paths with opportunities for professional growth
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives

Awards

• Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
• Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility