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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

 

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Meta Title:
Clinical Data Programming Lead SAS/RAVE Job Chennai

Meta Description:
Apply for Clinical Data Programming Lead at ICON in Chennai/Bangalore. 5+ yrs experience in SAS, Medidata Rave, clinical data integration. Hybrid role.

Meta Keywords:
clinical data programming lead, SAS programming job Chennai, Medidata Rave programmer, clinical trial data integration, Veeva CDMS, clinical data management jobs India, ICON clinical research jobs, hybrid pharma jobs Chennai


Job Summary

Join ICON plc as a Clinical Data Programming Lead in Chennai/Bangalore (Hybrid). This role is ideal for pharma professionals with 5+ years of clinical data programming expertise, proficient in SAS and EDC systems like Medidata Rave and Veeva CDMS. Lead critical data integration projects connecting Electronic Data Capture (EDC), CTMS, and payment entitlement systems, ensuring quality and timely delivery in clinical research.


Responsibilities

  • Lead programming and delivery of data integration between EDC, CTMS, and payment systems (APECS).

  • Support and act as backup for the Investigator Payments Group (IPG) Manager.

  • Manage multiple projects to meet timelines and quality standards.

  • Oversee specification development, programming, validation, and QA of study data deliverables.

  • Serve as SME and lead for Patient Data Integration (PDI) on eligible studies.

  • Maintain automated schedules and support systems for programming deliverables.

  • Provide technical oversight and mentorship to Clinical Data Programmers.

  • Troubleshoot and resolve programming or system integration issues.


Required Skills & Qualifications

  • 5+ years of clinical data programming and delivery experience.

  • Proven expertise in SAS programming.

  • Familiarity with extracting data from EDC systems, especially Medidata Rave and Veeva CDMS.

  • Strong knowledge of clinical data programming development lifecycle.

  • Excellent problem-solving, organizational, prioritization, and communication skills.

  • Ability to manage multiple tasks and perform with minimal supervision.

  • Bachelor’s degree in information systems, science, or related discipline (or equivalent experience).


Perks & Benefits

  • Competitive salary (exact compensation range not specified).

  • Annual leave entitlements and health insurance plans for employees and families.

  • Robust retirement planning options.

  • Global Employee Assistance Program (LifeWorks) offering 24/7 wellness support.

  • Life assurance coverage.

  • Flexible country-specific benefits such as childcare vouchers, bike purchase schemes, gym discounts, subsidized travel passes, and health assessments.


Company Description

ICON plc is a global leader in clinical research and healthcare intelligence. Dedicated to innovation and inclusivity, ICON empowers its workforce to transform clinical development and deliver life-changing healthcare solutions worldwide.


Work Mode

Hybrid — Chennai/Bangalore office-based with flexible remote work options.


Call to Action

Ready to take the lead in clinical data programming and make an impact in pharmaceutical research? Apply now for the Clinical Data Programming Lead role at ICON and join a dynamic team shaping the future of healthcare!