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Lead Clinical Data Science Programmer

5-8 years
Not Disclosed
10 July 18, 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

 

Lead Clinical Data Science Programmer – ICON, Bangalore (On-site)

Job Summary

ICON plc is hiring a Lead Clinical Data Science Programmer for its on-site Bangalore location. This role plays a pivotal part in enhancing global clinical data review by developing, maintaining, and delivering standardized and custom reports. You’ll translate reporting needs into powerful analytics solutions using tools like JReview, Spotfire, SAS, and SQL, collaborating with cross-functional stakeholders to ensure clinical data quality and compliance. Ideal for professionals with a strong foundation in clinical data science, programming, and reporting tools within the pharmaceutical or biotech industry.


Key Responsibilities

  • Develop and maintain global standard data review reports (e.g., patient profiles, reconciliation reports)

  • Design specifications and deploy reports across platforms like JReview, Spotfire, SAS

  • Generate integrated clinical data review reports including eCOA, CRF, and biomarker data

  • Update metadata definitions within MDR systems

  • Provide training to end-users based on roles and reporting tools

  • Create compliance and metrics reports to support regulatory and operational needs

  • Collaborate with clinical teams to identify report requirements and develop custom solutions

  • Contribute to SOPs, working procedures, and process documentation


Required Skills & Qualifications

  • Bachelor’s degree in Biology, Computer Science, Data Management, or related field

  • 5–8 years of data management experience in the pharmaceutical industry

  • 5+ years of experience using reporting tools such as JReview, Spotfire, SAS, SQL, Tableau, Qlik

  • Proficiency in SQL scripting, advanced queries, and stored procedures

  • Understanding of FDA/ICH clinical data guidelines, regulatory compliance, and computerized systems in clinical trials

  • Strong problem-solving, collaboration, and communication skills

  • Experience with EDC (Rave) systems is a plus


Perks & Benefits

  • Competitive industry salary (exact compensation not specified)

  • Annual leave entitlements

  • Multiple health insurance plans for individuals and families

  • Retirement planning support

  • Life assurance and access to global Employee Assistance Program (TELUS Health)

  • Flexible, country-specific optional benefits: childcare vouchers, gym discounts, bike schemes, subsidized travel, and more


Company Description

ICON plc is a leading global Clinical Research Organization (CRO) committed to delivering innovation and excellence in clinical development. With a robust biometrics and data-driven approach, ICON partners with top pharmaceutical and biotech companies to bring life-saving therapies to market efficiently and compliantly.


Work Mode

On-site – Bangalore, India
Remote Option – Not available
Open to Freshers – No


Call-to-Action

Ready to lead clinical data innovation in a world-class CRO? Apply now to join ICON in Bangalore and shape the future of pharmaceutical data reporting.