Programmer Analyst

Thermo Fisher Scientific India Pvt Ltd; Bengaluru; On-site; INR 900,000 - 1,300,000; Full time

Job summary

Thermo Fisher Scientific India Pvt Ltd in Bengaluru seeks an experienced SAS programmer to transfer, combine, and summarize data from multiple sources. You will generate and validate listings, tables, figures, and reports for clinical trial data, including lab, vital signs, imaging, QoL, and adverse events.

The role requires a Master’s or related bachelor’s degree and at least 4 years of SDTM/ADaM programming experience, with strong English communication and attention to detail.

Qualifications

• Master’s degree in CS, statistics, biostatistics, mathematics, or a related field; or a bachelor’s degree in a related field.
• At least 4 years of hands-on programming experience in SDTM or ADaM.
• Strong written and verbal communication in English; attention to detail.

Responsibilities

• Transfer, combine, and summarize data from multiple sources and systems using SAS and established tools.
• Generate and validate clinical listings, tables, figures, reports, and other outputs.
• Prepare and analyze clinical trial data including laboratory, vital signs, tumor response, imaging, QoL and adverse event data.
• Collaborate with researchers and multidisciplinary project teams to propose suitable technology solutions.
• Develop customized code using existing tools to produce or validate outputs.
• Mentor study teams and contribute to SOPs and training materials.
• Build programming and pharmaceutical knowledge through learning events and departmental documents.

Skills

SAS

SQL

ADaM/SDTM

English communication

Education

Masters in CS/Statistics

Bachelor in related field

Job description

What You’ll Do

Complete programming tasks assigned by study team leads. This includes creating, running, maintaining, and validating programs that transfer, combine, and summarize data from different sources and systems. Use SAS and established tools and processes to generate and validate clinical listings, tables, figures, reports, and other outputs. Prepare and analyze clinical trial data, including laboratory, vital signs, tumor response, imaging, quality-of-life, well-being questionnaire, and adverse event data. Work with researchers and multidisciplinary project teams to understand problems and recommend suitable technology solutions and programming strategies. Develop customized code using existing tools and applications to produce or validate clinical research and technical outputs. Contribute to multidisciplinary study teams and, with management oversight and review, begin supporting lead programming activities. Follow departmental work practices and standard operating procedures, and contribute to informal training materials. Build your programming, technology, clinical trial, and pharmaceutical industry knowledge through mentoring, learning events, and contributions to departmental documents and best-practice materials.

Education and Experience

A master’s degree in computer science, statistics, biostatistics, mathematics, or a related field; or a bachelor’s degree in a related field, or an equivalent relevant academic or vocational qualification. At least 4 years of hands-on programming experience in either SDTM or ADaM . Years of experience indicate the typical time needed to develop the knowledge and skills for the role. They are not the sole factor in determining job classification or selection.

Knowledge, Skills, and Abilities

Solid understanding of one or more programming languages. Familiarity with relational database structures and complex data systems. Strong attention to detail and problem-solving skills. Clear written and verbal communication skills, with proficiency in English. Ability to organize and manage multiple assignments with challenging timelines. Positive, collaborative approach and demonstrated initiative. Strong organizational skills and adaptability when priorities change.

Working Conditions

Work is performed in an office environment with exposure to electrical office equipment. Occasional travel to site locations, including domestic and international travel, may be required.

Why Join Us?

At Thermo Fisher Scientific, you’ll join a global team committed to innovation and scientific excellence. You’ll work in a collaborative environment that supports professional development and gives you the opportunity to contribute to meaningful work.