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Senior Lead Clinical Data Science Programmer

2+ years
Not Disclosed
10 June 26, 2025
Job Description
Job Type: Hybrid 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 Clinical Data Science Programmer – Bangalore/Chennai (Hybrid)

Job Summary

ICON plc is hiring a Senior Clinical Data Science Programmer in Bangalore or Chennai (Hybrid). Join one of the leading global CROs and work directly with global pharma partners to drive data standards in clinical trials. This role involves designing and implementing clinical metadata standards for data collection (Rave eDC, CRFs) and delivery (SDTM, define.xml) to improve quality, efficiency, and compliance across trials. Ideal for professionals with 2+ years in clinical data standards, programming, and metadata management.


Key Responsibilities

  • Design and manage metadata standards for clinical data collection and delivery.

  • Implement standard CRFs, COAs, validation rules, and integrations in Medidata Rave eDC.

  • Annotate CRFs with SDTM-compliant metadata for regulatory readiness.

  • Create and support standards content such as SDTM, define.xml, DTA, and metadata mapping.

  • Advise clinical data management and programming teams on standards adoption.

  • Maintain metadata traceability and lineage across systems and studies.

  • Collaborate with cross-functional teams including statisticians, physicians, and CDISC working groups.

  • Ensure inspection-ready documentation for all standards development activities.


Required Skills & Qualifications

  • Bachelor’s degree in Life Sciences, Computer Science, or related field.

  • Minimum 2 years of experience in clinical data management, data standards, or clinical programming.

  • Hands-on experience with Medidata Rave eDC (for data collection roles).

  • Proficiency in SAS programming; exposure to SAS LSAF is a plus.

  • Strong understanding of CDISC standards: SDTM, CDASH, controlled terminology, and define.xml.

  • Experience with Pinnacle 21 is an added advantage.

  • Excellent communication skills and ability to manage multiple priorities.

  • Strong documentation and organizational skills.


Perks & Benefits

  • Competitive salary package

  • Generous annual leave entitlements

  • Comprehensive health insurance plans for you and your family

  • Retirement planning support and life assurance

  • Access to TELUS Health Employee Assistance Programme

  • Flexible optional benefits including:

    • Gym memberships

    • Bike purchase schemes

    • Childcare vouchers

    • Subsidized travel

    • Preventive health assessments


Company Description

ICON plc is a globally recognized Clinical Research Organization (CRO), providing full-service development solutions to the pharmaceutical, biotech, and medical device industries. With a focus on clinical data integrity, regulatory compliance, and biometric innovation, ICON delivers top-tier research support across every therapeutic area.


Work Mode

Hybrid – Location: Bangalore or Chennai, India


Call-to-Action

Are you ready to elevate your career in clinical data programming with one of the world’s leading CROs? Apply today to join ICON and play a critical role in advancing data standards in global clinical trials.
Submit your application now and be part of the future of healthcare data innovation.