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Clinical Data Programming Lead

5+ years
Not Disclosed
10 May 16, 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

Job Title: Clinical Data Programming Lead
Location: Chennai / Bangalore (Hybrid)
Job ID: JR122637
Department: Clinical Data Management, Programming – ICON Full Service & Corporate Support


Company Overview:

ICON plc is a global leader in clinical research and healthcare intelligence. We are committed to fostering a culture that values inclusion, innovation, and professional growth. Join us as we shape the future of clinical development with cutting-edge solutions and collaborative excellence.


Role Summary:

As a Clinical Data Programming Lead, you will be responsible for delivering and overseeing data integration solutions involving Electronic Data Capture (EDC) systems, Clinical Trial Management Systems (CTMS), and payment entitlement calculation platforms (APECS). You will also provide programming support to the Investigator Payments Group (IPG) and act as a backup to the IPG Manager.


Key Responsibilities:

  • Lead programming activities for Patient Data Integration (PDI) across new eligible studies

  • Develop, validate, and oversee data deliverables from clinical studies

  • Setup and maintain programming deliverables, including automated scheduling systems

  • Troubleshoot and resolve programming/system integration issues as needed

  • Provide mentorship, oversight, and quality assurance for other Clinical Data Programmers

  • Ensure compliance with project timelines and ICON’s quality standards

  • Participate in specification development and continuous improvement of programming processes


Experience & Skills Required:

  • Minimum 5 years of experience in clinical data programming and delivery

  • Proven experience with SAS programming

  • Familiarity with EDC systems, particularly Medidata Rave and Veeva CDMS

  • Strong problem-solving skills and ability to manage multiple timelines

  • Advanced knowledge of the clinical data programming lifecycle

  • Excellent communication skills (written and verbal)

  • Ability to work independently and collaboratively

  • Quick adaptability to new tools, technologies, and methodologies


Educational Requirements:

  • Bachelor’s degree in Information Systems, Life Sciences, or related discipline

  • Equivalent relevant experience will also be considered


What ICON Offers:

ICON offers a comprehensive benefits package and a dynamic work environment focused on personal and professional growth:

  • Competitive salary and leave entitlements

  • Health insurance plans tailored to your family’s needs

  • Retirement savings options with strategic planning support

  • 24/7 access to LifeWorks Global Employee Assistance Programme

  • Life assurance and wellness initiatives

  • Country-specific perks including:

    • Childcare vouchers

    • Bike purchase schemes

    • Discounted gym memberships

    • Subsidized travel passes

    • Health assessments

Learn more about our benefits here: ICON Careers Benefits


Diversity & Inclusion at ICON:

ICON is committed to a discrimination-free workplace and promotes an inclusive environment. All qualified applicants will receive equal consideration for employment. If you require reasonable accommodations to participate in the application or hiring process, please submit a request here.

Not sure you meet all the criteria? Apply anyway — your unique skills might be exactly what we need.