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Senior Programmer Analyst

5-8 years
Not Disclosed
10 June 11, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, 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, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Senior Programmer Analyst (5–8 years experience)

Location: Bangalore, India
Company: Fortrea
Work Mode: Hybrid (On-site/Remote)


Job Summary

Fortrea is hiring a Senior Programmer Analyst for its Data Management & Data Science division in Bangalore. This role focuses on developing and implementing solutions for EDC tools, SAS programming, SDTM dataset creation, and visual analytics using Spotfire/Tableau. The position demands expertise in leading clinical data programming activities, handling post-production changes, and performing data reconciliations for global clinical trials.


Key Responsibilities

  • Lead development of solutions for technical services issues related to EDC tools (Medidata RAVE, Oracle Inform) and SAS programming.

  • Develop and validate complex SAS/SDTM datasets and manage external data reconciliations.

  • Design and develop dashboards using Spotfire or Tableau for clinical data visualization.

  • Perform post-production changes to EDC databases and SAS programs (e.g., edit checks, protocol deviations).

  • Act as Subject Matter Expert (SME) and point of contact for EDC and SAS-related technical services.

  • Provide programming support for SDTM/Client standard datasets development and maintenance.

  • Plan and oversee all programming activities including resource estimation and quality control.

  • Lead peer review and quality control of study designs.

  • Stay current with new EDC product developments to enhance system efficiency.

  • Support project documentation and contribute to the design of eCRFs and other study materials.


Required Skills & Qualifications

  • Bachelor’s degree in Life Sciences, Health Sciences, Information Technology, or related fields.

  • 5–8 years of relevant experience in data management, SAS programming, or visual analytics (Spotfire/Tableau).

  • Strong problem-solving and analytical skills.

  • Proficiency in EDC tools (Medidata RAVE, Oracle Inform) and SAS programming.

  • Experience with SDTM domains, data standards, and reconciliation processes.

  • Familiarity with the clinical trial process and data management operations.

  • Excellent communication skills and the ability to work independently or as part of a team.

  • Strong organizational skills with a focus on meeting deadlines and maintaining quality.


Perks & Benefits

  • Opportunity to work with a globally recognized CRO.

  • Involvement in diverse therapeutic areas and cutting-edge clinical technologies.

  • Hybrid work flexibility.

  • Training and development programs for continuous learning.

  • Inclusive and collaborative workplace culture.


Company Description

Fortrea is a global Contract Research Organization (CRO) offering clinical development and technology solutions across 20+ therapeutic areas. Operating in over 100 countries, Fortrea partners with pharmaceutical, biotechnology, and medical device companies to drive innovation and deliver transformative therapies.


Work Mode

Hybrid (Bangalore, India)


Call to Action

Ready to lead clinical data programming for global trials? Apply today to join Fortrea and make a meaningful impact on patient-focused clinical research.