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.
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