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Clinical Data Programming Lead - Sas/Rave Programming

5+ years
Not Disclosed
10 June 5, 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

 

Meta Title

Clinical Data Programming Lead - SAS/RAVE | ICON Chennai

Meta Description

Join ICON as Clinical Data Programming Lead in Chennai/Bangalore. Lead SAS & EDC data integration, manage projects, and support clinical trial data delivery.

Meta Keywords

clinical data programming lead, sas programming jobs india, rave clinical data management, clinical trial programming, data integration, icon jobs chennai, clinical data jobs india, edc programming lead


Clinical Data Programming Lead - SAS & RAVE | ICON plc, Chennai/Bangalore (Hybrid)

Location: Chennai / Bangalore
Employment Type: Full-Time
Work Mode: Hybrid (Office & Remote)


Job Summary

ICON plc, a global leader in healthcare intelligence and clinical research, is seeking a Clinical Data Programming Lead experienced in SAS and Electronic Data Capture (EDC) systems, including Medidata Rave and Veeva CDMS. This hybrid role based in Chennai or Bangalore offers the opportunity to lead data integration between EDC, CTMS, and payment systems while managing multiple clinical data projects. Ideal for professionals with 5+ years in clinical data programming, this role focuses on quality, timelines, and innovation in clinical trial data management.


Responsibilities

  • Lead programming and oversight of clinical data integration between EDC, CTMS, and payment entitlement systems (APECS)

  • Act as backup for the Investigator Payments Group (IPG) Manager, supporting team leadership and project delivery

  • Manage multiple clinical data programming projects ensuring compliance with timelines and quality standards

  • Develop specifications, program, validate, and assure quality of clinical study data deliverables

  • Serve as Subject Matter Expert (SME) for Patient Data Integration (PDI) across eligible studies

  • Oversee setup, monitoring, and maintenance of automated programming schedules and support systems

  • Provide technical guidance, mentorship, and quality assurance for clinical data programmers

  • Troubleshoot and resolve programming and system integration issues effectively


Required Skills & Qualifications

  • Bachelor’s degree in Information Systems, Science, or related field, or equivalent experience

  • Minimum 5 years’ clinical data programming experience with SAS and EDC systems

  • Proven experience with Medidata Rave and Veeva CDMS data extraction and manipulation

  • Strong understanding of clinical data programming lifecycle and data validation processes

  • Excellent problem-solving skills and ability to manage multiple projects simultaneously

  • Strong verbal and written communication skills in English

  • Ability to work independently and as part of a collaborative team

  • Proficient in troubleshooting programming and integration issues

  • Skilled in time management, organization, and prioritization


Perks & Benefits

  • Competitive salary (not explicitly stated) with performance-based rewards

  • Various annual leave entitlements for work-life balance

  • Comprehensive health insurance for employees and dependents

  • Retirement planning schemes to secure your future

  • Access to Global Employee Assistance Programme (LifeWorks) for personal and family support

  • Life assurance coverage

  • Flexible country-specific benefits like childcare vouchers, gym discounts, and subsidized travel passes


Company Description

ICON plc is a leading global Contract Research Organization (CRO) specializing in clinical development and healthcare solutions. With a commitment to innovation, quality, and inclusion, ICON supports pharmaceutical, biotech, and medical device companies in advancing clinical trials and bringing new therapies to market worldwide.


Work Mode

Hybrid – Combination of remote and on-site work in Chennai or Bangalore office.


Call to Action

If you have a strong background in clinical data programming and are ready to lead complex data integration projects within a global clinical research leader, apply now. Visit ThePharmaDaily.com to submit your application and take your clinical programming career to the next level with ICON.