Meta Title
Senior Statistical Programmer I - ICON India | Clinical Programming
Meta Description
Join ICON as Senior Statistical Programmer I in Bangalore, Chennai & Trivandrum. Lead CDISC ADaM programming, manage projects, and enhance clinical data analysis.
Meta Keywords
senior statistical programmer india, clinical programming jobs india, CDISC ADaM programming, statistical programming jobs, ICON jobs india, clinical data analysis, statistical programmer bangalore, statistical programmer chennai
Senior Statistical Programmer I - ICON plc | Bangalore, Chennai & Trivandrum (Office or Home)
Location: Bangalore, Chennai, Trivandrum
Employment Type: Full-Time
Work Mode: Hybrid (Office or Remote)
Job Summary
ICON plc, a global leader in healthcare intelligence and clinical research, invites experienced professionals to join as Senior Statistical Programmer I. This role is ideal for candidates with 6+ years of experience in clinical statistical programming, specializing in CDISC ADaM standards. You will lead multi-disciplinary teams, develop and validate statistical programs, and contribute to clinical trial data analysis. This position offers a flexible work mode (office or home) across multiple Indian cities, fostering career growth within a pioneering healthcare research environment.
Responsibilities
Lead and manage multi-disciplinary teams on assigned clinical programming projects
Develop, maintain, and validate standard data structures and statistical software programs
Design and implement departmental macros that are well-documented, maintainable, and user-friendly
Monitor program development and validation procedures to ensure quality and compliance
Assist in training statisticians and programmers to enhance data analysis capabilities
Produce analysis datasets, tables, listings, and graphs (TFLs) with focus on CDISC ADaM standards
Required Skills & Qualifications
Bachelor’s degree in a quantitative or scientific discipline; Master’s or PhD preferred
Minimum 6 years of relevant clinical statistical programming experience
Strong expertise in creating and validating CDISC ADaM analysis datasets
Proficient in statistical programming tools and technologies (e.g., SAS)
Excellent leadership, communication, and project management skills
Ability to design maintainable and validated macros and programs
Experience in clinical trial data reporting and statistical output generation
Perks & Benefits
Competitive salary (exact compensation not specified) with performance incentives
Various annual leave entitlements promoting work-life balance
Comprehensive health insurance plans for employees and families
Retirement planning and savings schemes tailored for long-term security
Access to Global Employee Assistance Programme (LifeWorks) offering 24/7 support
Life assurance coverage for peace of mind
Flexible country-specific benefits including childcare vouchers, gym discounts, and travel subsidies
Company Description
ICON plc is a premier global Contract Research Organization (CRO) focused on clinical development, healthcare intelligence, and drug safety. ICON supports pharmaceutical and biotech clients worldwide to streamline clinical trials, accelerate drug development, and improve patient outcomes through cutting-edge technology and data expertise.
Work Mode
Hybrid: Candidates can choose to work remotely or from ICON offices in Bangalore, Chennai, or Trivandrum.
Call to Action
If you have strong clinical programming experience and a passion for driving innovation in clinical data analysis, apply now at ThePharmaDaily.com. Join ICON to advance your career and contribute to shaping the future of clinical research.
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