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 is seeking a highly skilled Senior Programmer III to join our clinical data programming team in India. This is an exciting opportunity for experienced SAS programmers to contribute to high-quality clinical trial outputs, support junior team members, and take ownership of complex programming tasks.
In this role, you will work with SDTM and ADaM datasets, ensure compliance with CDISC standards, and help deliver accurate, timely, and validated clinical data outputs that inform key regulatory and business decisions. You will thrive in a hybrid work environment, collaborating with cross-functional teams and guiding junior programmers.
This position is ideal for candidates with a strong statistical programming background, experience in clinical research, and a desire to grow into leadership and mentoring roles.
Key Responsibilities
Develop, validate, and deliver high-quality datasets and statistical outputs using SAS programming, SDTM, and ADaM standards.
Utilize Pinnacle21 and other tools to ensure CDISC compliance.
Mentor and support junior programmers, providing guidance, reviewing work, and fostering skill development.
Take ownership of study-level programming activities, including lead responsibilities where appropriate.
Communicate clearly with cross-functional teams and support smooth project execution in a hybrid setup.
Identify potential issues proactively and implement solutions to maintain timely and accurate deliverables.
Required Qualifications & Skills
MSc or equivalent in Statistics, Mathematics, or a related quantitative field with strong statistical coursework.
5–8 years of experience in statistical programming within clinical research or related data-driven environments.
Strong SAS programming skills, including experience in coding, debugging, and validation.
Hands-on experience with CDISC standards (SDTM, ADaM) and compliance tools like Pinnacle21.
Experience mentoring or supporting junior programmers and reviewing deliverables.
Excellent analytical, problem-solving, and organizational skills.
Strong written and verbal communication skills.
Exposure to additional programming languages such as R or Python is a plus.
Preferred Qualifications
Previous experience in pharmaceutical, biotechnology, or CRO settings.
Familiarity with global regulatory standards (ICH/GCP).
Proven ability to manage multiple tasks, meet deadlines, and maintain high-quality output.
Why Join Quanticate?
Quanticate is a global data-focused CRO delivering innovative clinical programming, biostatistics, and data management solutions. By joining us, you will:
Work on complex global clinical trials, contributing to critical data outputs.
Advance your technical expertise and leadership skills through mentoring and hands-on exposure.
Explore emerging programming languages and analytics tools to broaden your skillset.
Thrive in a culture that emphasizes initiative, ownership, and continuous improvement.
Collaborate with top pharmaceutical companies and biotech innovators, impacting therapies worldwide.
Benefits & Perks
Competitive salary and performance-based incentives.
Flexible working hours and hybrid work setup.
Paid holidays, including annual, sick, casual leave, and bank holidays.
Medical insurance for employees and immediate family.
Gratuity and accidental coverage.
Professional development opportunities including mentoring, coaching, e-learning, and job shadowing.
How to Apply
Qualified candidates will be considered based on merit and experience. Quanticate does not request 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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