Programmer Analyst II

Thermo Fisher Scientific

. Perform programming activities supporting the statistical and computational needs of research projects .

Posted 11/11/2026full-timeBangalore • IndiaMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in SAS programming, clinical trial data analysis, and the application of clinical data standards such as SDTM and ADaM. Capable of collaborating with multidisciplinary teams to develop technology-based solutions and manage complex datasets effectively.

Highest-signal resume keywords

SAS Programming ExperienceSDTM DevelopmentADaM DevelopmentClinical Trial ProgrammingData Analysis

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

SASStatistical ProgrammingData ValidationClinical Listings DevelopmentData ManagementDatabase ManagementData AnalysisReport GenerationClinical Trial Data StandardsBioinformatics Programming

Soft Skills

Effective CommunicationOrganizational SkillsCollaborative ApproachAdaptabilityInitiative

Industry Keywords

Clinical TrialsPharmaceutical IndustryRelational DatabasesData SystemsMultidisciplinary Teams

About the role

Key responsibilities & impact

Perform programming activities supporting the statistical and computational needs of research projects
Prepare and analyze clinical trial patient datasets
Create, execute, maintain, and validate programs using SAS and other standard tools and processes
Transfer data across data management systems and operating systems
Combine data from differently structured sources and generate summary data
Generate reports and work with multiple databases
Develop and validate programs producing clinical listings, tables, and figures (TLFs)
Analyze laboratory, vital signs, tumor response, imaging, quality of life, wellbeing questionnaire, and adverse events data
Apply clinical data standards including SDTM and ADaM
Work with researchers and multidisciplinary project teams to recommend technology-based solutions and computational strategies
Develop customized code for clinical bioinformatics and technical outputs
Contribute to study teams under the guidance of a lead programmer
Begin assisting with lead programming activities under management oversight and review
Follow departmental working practice documents and standard operating procedures
Contribute to training materials and departmental documents
Build knowledge of programming technologies, clinical trials, and the pharmaceutical industry
Work with mentors, attend presentations and training events, and assist with implementing best practices

Requirements

What you’ll need

Master’s degree in Computer Science, Statistics, Biostatistics, Mathematics, or a related field; or Bachelor’s degree in one of these fields, or equivalent, with a relevant formal academic or vocational qualification
At least 4 years of end-to-end SAS programming experience
Hands-on SDTM, ADaM, and TLF development and validation experience
Solid understanding of SAS and clinical trial programming
Experience working with SDTM, ADaM, and TLFs
Understanding of relational databases and complex data systems
Effective written and verbal communication skills in English
Ability to organize and manage multiple assignments with challenging timelines
Positive, collaborative approach and demonstrated initiative
Good organizational skills and ability to adapt to changing priorities
Willingness/ability to work in an office environment
Ability to accommodate occasional drives to site locations and occasional domestic or international travel

Benefits

Comp & perks

Global team environment
Opportunities to develop programming skills
Mentorship
Presentations and training events
Informal training materials and departmental documents
Professional development in programming technologies, clinical trials, and the pharmaceutical industry
Exposure to best practices and scientific innovation