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

Programmer Analyst Ii

Thermo Fisher Scientific
2+ years
Not Disclosed
Bangalore, India
9 May 29, 2026
Job Description
Job Type: Full Time Hybrid Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: 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

Programmer Analyst II

Company: Thermo Fisher Scientific
Work Schedule: Standard (Monday–Friday)
Work Environment: Office-Based


About the Role

Thermo Fisher Scientific is seeking a Programmer Analyst II to support bioinformatics programming and statistical computing activities for clinical research projects.

In this role, you will work as part of a study team under the guidance of a lead programmer while also taking ownership of lead activities for selected studies. You will contribute to clinical trial data analysis, statistical programming, and data integration efforts across multidisciplinary research teams.


Key Responsibilities

1. Statistical & Bioinformatics Programming

  • Perform programming tasks assigned by study project leads.

  • Independently create, execute, maintain, and validate programs for:

    • Data transfer across multiple systems

    • Data integration and transformation

    • Summary data generation

    • Report generation

    • Database combination and validation

  • Generate and validate:

    • Listings

    • Tables

    • Figures (LTFs)

  • Use:

    • SAS

    • Standard programming tools and processes


2. Clinical Trial Data Analysis

  • Prepare and analyze clinical trial datasets, including:

    • Laboratory data

    • Vital signs data

    • Tumor response data

    • Imaging data

    • Quality of life questionnaire data

    • Adverse events data

  • Collaborate with:

    • Researchers

    • Clinical teams

    • Multidisciplinary project teams

  • Recommend technology-based and computational solutions for research projects.


3. Development & Validation

  • Develop customized programming code to:

    • Utilize existing tools and applications

    • Generate outputs

    • Validate outputs for clinical and technical use

  • Ensure quality and accuracy of programming deliverables.


4. Study Leadership Support

  • Act as the programming lead for simple to moderately complex studies.

  • Support study delivery and programming responsibilities.

  • Gain practical understanding of the lead programmer role through mentorship and project participation.

  • Work under close supervision on lead programming assignments.


5. Learning & Professional Development

  • Expand expertise in:

    • Programming

    • Bioinformatics tools

    • Clinical trials

    • Pharmaceutical industry practices

  • Participate in:

    • Training sessions

    • Presentations

    • Teaching events

  • Contribute to:

    • Informal training materials

    • Best practice documents

    • Departmental SOPs and policies


Educational Qualifications

Required Education

Option 1

  • Master’s degree (MS/MA) in:

    • Computer Science

    • Statistics

    • Biostatistics

    • Mathematics

    • Related field

Option 2

  • Bachelor’s degree in:

    • Computer Science

    • Statistics

    • Biostatistics

    • Mathematics

    • Related field

  • Equivalent academic or vocational qualification may also be considered.


Experience Requirements

  • Minimum 2 years of relevant experience in:

    • Statistical programming

    • Bioinformatics

    • Clinical research programming

    • Data systems management


Required Skills & Competencies

Technical Skills

  • Solid understanding of one or more programming languages.

  • Experience with:

    • SAS programming

    • Relational database structures

    • Complex data systems

  • Ability to work with clinical trial datasets and analytical outputs.


Analytical & Organizational Skills

  • Strong attention to detail.

  • Good problem-solving capabilities.

  • Ability to organize and manage multiple assignments under tight timelines.

  • Adaptability to changing priorities and project requirements.


Communication & Collaboration

  • Good written and verbal communication skills.

  • Proficiency in English.

  • Positive attitude and strong teamwork abilities.

  • Demonstrated initiative and motivation.


Working Conditions

  • Office-based work environment.

  • Exposure to standard office equipment.

  • Occasional travel:

    • Domestic

    • International

  • Occasional visits to site locations.


Why Join Thermo Fisher Scientific?

At Thermo Fisher Scientific, you’ll become part of a global organization dedicated to:

  • Scientific innovation

  • Research excellence

  • Collaboration

  • Professional development

  • Meaningful healthcare impact

You’ll work in a dynamic environment where learning and teamwork are encouraged, and where your contributions directly support scientific breakthroughs and improved patient outcomes worldwide.


About Thermo Fisher Scientific

Thermo Fisher Scientific is a global leader in scientific research, healthcare, and laboratory solutions, helping customers accelerate innovation and improve health outcomes around the world.