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Lead Clinical Data Science Programmer

5-8 years
Not Disclosed
10 Nov. 12, 2025
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences 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: Lead Clinical Data Science Programmer

Locations:

Bangalore | Chennai | Trivandrum | Bengaluru

Job Requisition ID: JR138014

Department:

ICON Strategic Solutions – Clinical Data Science

Job Type:

  • Employment Type: Full-time (6-Month Contract)

  • Work Arrangement: Office-based

  • Functional Area: Clinical Data Programming / Data Science

Experience Level:

  • Mid to Senior Level

  • Relevant experience in clinical data reporting, analytics, and programming (preferably with SQL, SAS, R, or Python).


About the Role

ICON plc is a world-leading healthcare intelligence and clinical research organization committed to advancing the future of clinical development.

We are seeking a Lead Clinical Data Science Programmer to join our dynamic team. In this role, you will be responsible for designing and developing innovative data programming solutions to support complex clinical trials. You will lead data analysis, reporting, and visualization efforts, enabling data-driven insights that shape the development of new therapies.


Key Responsibilities

  • Act as the primary point of contact for system programming activities during study setup and execution.

  • Translate clinical study reporting requirements into technical specifications, creating customized data review and reporting solutions using JReview, Spotfire, and SAS.

  • Develop and maintain global standard reports integrating CRF, biomarker, and eCOA data sources.

  • Design and optimize SQL queries, stored procedures, and analytical dashboards to enhance data accessibility.

  • Support the development and maintenance of SOPs, working procedures, and internal documentation to ensure compliance and standardization.

  • Manage metadata and MDR system updates, ensuring accuracy and alignment with project timelines.

  • Deliver training sessions and generate compliance and metrics reports to support data governance.

  • Identify project risks, propose mitigation strategies, and maintain clear stakeholder communication.


Profile Expectations

  • Strong understanding of clinical trial processes, drug development life cycle, and regulatory frameworks (FDA, ICH, GCP).

  • Proven expertise in clinical data reporting and analytics with advanced proficiency in SQL.

  • Working knowledge of SAS, R, Python, and visualization platforms such as Spotfire or JReview.

  • Familiarity with EDC systems (e.g., Medidata Rave) and computerized system validation principles.

  • Excellent communication, organizational, and leadership skills within a matrixed, cross-functional environment.

  • Strong analytical mindset, capable of problem-solving and driving innovation in data management.

  • Experience collaborating with stakeholders, gathering requirements, and translating business needs into technical deliverables.


What ICON Can Offer You

ICON recognizes that its success depends on the excellence of its people. The company fosters an inclusive, performance-driven culture focused on innovation and well-being.

Benefits include:

  • Competitive salary and contract benefits

  • Various annual leave entitlements

  • Comprehensive health insurance for you and your family

  • Attractive retirement planning options

  • Global Employee Assistance Programme (LifeWorks) with 24/7 access to support professionals

  • Life assurance

  • Flexible country-specific perks such as childcare vouchers, gym memberships, bike schemes, travel subsidies, and health assessments