Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Sr Programmer Analyst Ii

Thermo Fisher Scientific
3+ years
18-35 LPA
Bangalore, Remote, India, India
10 June 11, 2026
Job Description
Job Type: Full Time Hybrid Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance, Communication Skills, CPC Certified, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Senior Programmer Analyst

Company: Thermo Fisher Scientific
Department: Biostatistics / Statistical Programming / Bioinformatics
Work Schedule: Monday–Friday (Standard)
Work Environment: Office-Based
Job Type: Full-Time


Experience Level

  • MS/MSc/MA in Computer Science, Statistics, Biostatistics, Mathematics, Bioinformatics, or related field with 3+ years of relevant experience
    OR

  • Bachelor's Degree with 5+ years of relevant Statistical Programming experience

  • Senior Individual Contributor (IC) Level

  • Team Lead responsibilities on selected projects


Salary

Estimated market salary: ₹18–35 LPA CTC in India, with experienced SAS Programmers/Statistical Programmers in global CROs potentially earning ₹35–50 LPA.


Role Summary

The Senior Programmer Analyst is responsible for advanced statistical programming, clinical trial data processing, bioinformatics programming, and generation of analysis datasets, tables, listings, and figures (TLFs). The role serves as a lead programmer on moderately complex clinical studies while mentoring junior programmers and supporting global clinical trial projects.


Key Responsibilities

Statistical Programming

  • Develop and validate SAS programs.

  • Generate:

    • Tables

    • Listings

    • Figures (TLFs)

    • Analysis datasets

  • Support clinical trial reporting requirements.

  • Ensure programming quality and compliance.


Clinical Trial Data Management

  • Transfer and integrate data across multiple systems.

  • Combine datasets from various sources.

  • Create summary datasets for statistical analysis.

  • Support database integration and validation activities.


Lead Programmer Responsibilities

  • Act as Lead Programmer for selected studies.

  • Collaborate with project leaders and clients.

  • Define programming timelines and deliverables.

  • Coordinate programming activities within study teams.


Quality Control & Validation

  • Perform programming validation.

  • Conduct quality review of statistical outputs.

  • Ensure compliance with SOPs and industry standards.

  • Review programming deliverables from junior team members.


Project Management

  • Manage multiple assignments simultaneously.

  • Deliver projects within timelines and budget.

  • Support risk identification and mitigation.

  • Ensure contractual and client requirements are met.


Training & Mentoring

  • Train and guide junior programmers.

  • Provide technical support and knowledge sharing.

  • Assist with onboarding and skill development initiatives.


Departmental Contributions

  • Develop SOPs and best practices.

  • Create training materials.

  • Support business development and proposal activities.

  • Represent the organization at conferences and scientific meetings.


Required Qualifications

Education

  • MSc/MS/MA in:

    • Statistics

    • Biostatistics

    • Bioinformatics

    • Mathematics

    • Computer Science

    • Related disciplines

OR

  • Bachelor's degree with significant relevant experience.

Professional Experience

  • 3+ years (Master's degree holders)

  • 5+ years (Bachelor's degree holders)

  • Experience in:

    • Statistical Programming

    • Clinical Trials

    • Pharmaceutical Research

    • CRO Environment


Key Technical Skills

  • SAS Programming

  • Clinical Data Analysis

  • Statistical Programming

  • Data Validation

  • Relational Databases

  • Clinical Trial Reporting

  • Data Integration

  • Quality Control


Preferred Skills

  • CDISC Standards (SDTM, ADaM)

  • Clinical Trial Data Management

  • Biostatistics

  • Bioinformatics

  • SQL

  • R Programming (preferred)

  • Regulatory Submission Support


Soft Skills

  • Leadership

  • Analytical Thinking

  • Problem Solving

  • Project Management

  • Communication Skills

  • Mentoring & Coaching

  • Time Management

  • Stakeholder Management


Travel Requirement

  • Primarily office-based role.

  • Occasional domestic and international travel.

  • Potential attendance at client meetings, conferences, and project-related visits.


Ideal Candidate

A statistical programming professional with strong SAS expertise, clinical trial experience, and the ability to independently lead programming activities on global studies. The candidate should be comfortable mentoring junior programmers while delivering high-quality outputs in a regulated pharmaceutical research environment.


Career Path

  • Senior Programmer Analyst

  • Lead Statistical Programmer

  • Principal Statistical Programmer

  • Programming Manager

  • Associate Director – Statistical Programming

  • Director – Biostatistics & Programming