Senior Clinical Data Science Programmer (Rave & Custom Functions)
Locations: Chennai | Bangalore, India
Work Model: Office with Flex
Employment Type: Full-Time
Industry: Clinical Data Science | Clinical Data Programming | CRO
Company: ICON plc
Job Overview
ICON plc, a global leader in healthcare intelligence and clinical research, is hiring a Senior Clinical Data Science Programmer to support the design, development, and validation of advanced clinical data solutions. This role is critical to ensuring the accuracy, consistency, and regulatory compliance of complex clinical trial data across global studies.
The position is ideal for experienced clinical data programmers with strong expertise in Medidata Rave, custom function development, and CDISC standards, who are looking to take on technical leadership responsibilities within a high-performing CRO environment.
Key Responsibilities
Lead the design, development, and validation of clinical data science programming solutions for Phase I–IV clinical trials.
Develop and validate Rave custom functions, edit checks, and data transformation logic to support clinical data workflows.
Collaborate with biostatistics, clinical data management, and clinical operations teams to define data specifications and analysis requirements.
Program, validate, and review datasets, tables, listings, and figures (TLFs) in alignment with study protocols and regulatory expectations.
Ensure data integrity, traceability, and quality through robust validation and quality control processes.
Provide technical guidance and mentoring to junior programmers and contribute to best practices within the data science programming function.
Support inspection readiness by ensuring compliance with CDISC (SDTM, ADaM), ICH-GCP, and global regulatory standards.
Required Qualifications & Experience
Education:
Bachelor’s or higher degree in Computer Science, Data Science, Biostatistics, Statistics, Life Sciences, or a related discipline.
Experience:
Minimum 4–6 years of hands-on experience in clinical data programming within a CRO, pharmaceutical, or biotechnology organization.
Proven experience with Medidata Rave, including custom function development and validation.
Strong working knowledge of clinical trial data structures and CDISC standards (SDTM and ADaM).
Technical & Professional Skills:
Advanced programming and analytical skills with a strong focus on data accuracy and quality.
Experience supporting regulatory submissions and inspection-ready datasets.
Ability to manage multiple studies and priorities in a fast-paced, global environment.
Strong communication, problem-solving, and cross-functional collaboration skills.
Demonstrated ability to provide technical leadership and knowledge sharing within teams.
Why Join ICON
ICON offers a collaborative and inclusive workplace that values innovation, scientific rigor, and professional growth. Employees benefit from global exposure, continuous learning opportunities, and the chance to contribute to the development of life-changing therapies.
Benefits & Rewards
Competitive compensation aligned with global CRO benchmarks
Comprehensive health insurance coverage for employees and families
Generous annual leave and holiday policies
Retirement and long-term savings plans
Global Employee Assistance Program (TELUS Health)
Life assurance and flexible, country-specific benefits
Strong focus on work–life balance and employee well-being
Equal Opportunity Statement
ICON is an equal opportunity employer committed to diversity, inclusion, and accessibility. All qualified applicants will be considered without regard to race, religion, gender, sexual orientation, disability, or protected veteran status. Reasonable accommodations are available throughout the recruitment process.
Apply Now
If you are an experienced Clinical Data Science Programmer with strong Rave and custom function expertise, this is an opportunity to advance your career with a globally recognized CRO. Apply today through thepharmadaily.com and be part of ICON’s mission to improve patient outcomes worldwide.
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