Senior Programmer III – Clinical Data Programming
Locations: Bengaluru, Karnataka, India | Hyderabad, Telangana, India
Department: Programming / Biostatistics
Job ID: ATR2120
Experience Required: 5–8 years in statistical programming
Employment Type: Full-Time | Hybrid
Job Summary
Quanticate, a global leader in data-focused CRO services, is seeking an experienced Senior Programmer III to join our clinical programming teams in Bengaluru and Hyderabad. This role is ideal for SAS programmers with hands-on experience in clinical trial data, SDTM/ADaM standards, and CDISC compliance.
As a Senior Programmer III, you will take ownership of programming tasks, mentor junior team members, and contribute to high-quality outputs that drive critical decisions in global clinical research. This role offers a unique opportunity to grow your technical and leadership skills while working on complex clinical trial programs for pharmaceutical, biotechnology, and medical device clients worldwide.
Key Responsibilities
Develop, validate, and deliver SDTM and ADaM datasets using SAS programming, ensuring adherence to CDISC standards.
Utilize Pinnacle21 and other compliance tools to ensure accuracy and regulatory compliance.
Provide mentorship and guidance to junior programmers, reviewing their work and supporting skill development.
Take ownership of study-level programming activities, with opportunities for lead responsibilities.
Collaborate effectively with cross-functional teams in a hybrid work setup, maintaining communication and project continuity.
Identify issues proactively, communicate early, and help maintain project timelines and deliverables.
Qualifications & Skills
Educational Requirements:
MSc (or equivalent) in Statistics, Mathematics, or related quantitative field with strong statistical content.
Experience Required:
5–8 years of hands-on experience in statistical programming in clinical research or data-driven environments.
Strong SAS programming expertise, including writing, debugging, and validating complex code.
Practical experience with CDISC standards (SDTM, ADaM) and familiarity with Pinnacle21.
Experience mentoring or supporting junior programmers.
Preferred Skills:
Exposure to additional programming languages such as R or Python.
Knowledge of ICH/GCP guidelines and global clinical trial standards.
Strong analytical, problem-solving, and organizational skills.
Excellent written and verbal communication skills.
Why Join Quanticate?
Quanticate is a global, data-driven CRO delivering innovative solutions in clinical programming, biostatistics, and data management. By joining us, you will:
Work on highly complex clinical trials with global pharmaceutical and biotech clients.
Gain exposure to advanced programming practices, data standards, and regulatory compliance.
Grow into leadership roles, mentoring junior programmers and contributing to team development.
Access professional development opportunities, including mentoring, coaching, e-learning, and job shadowing.
Be part of a culture that values ownership, initiative, and continuous improvement.
Benefits
Competitive salary and performance-based incentives.
Flexible working hours with hybrid setup.
Paid annual, sick, casual, and bank holidays.
Comprehensive medical insurance for self and immediate family.
Gratuity and accidental coverage.
Learning and development opportunities to support career growth.
How to Apply
Qualified candidates will be considered on merit and experience. Quanticate does not request any payments or paid courses for recruitment. All legitimate communication will come exclusively from @quanticate.com.
Apply via Email: careers@quanticate.com
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