Statistical Programmer I – Clinical Data Science
Location: Hyderabad, Telangana, India
Department: Programming / Biostatistics
Job ID: ATR2113
Experience Required: Entry-level (0–2 years)
Employment Type: Full-Time | On-Site
Job Summary
Kickstart your career in clinical data science with a role that merges statistics and programming in a real-world clinical research environment. We are seeking a highly motivated Statistical Programmer I to support statistical and programming teams at Quanticate in Hyderabad.
In this entry-level role, you will gain hands-on experience in the development and validation of datasets, statistical outputs, and clinical trial reports. You will work under the mentorship of experienced professionals, contributing to global clinical trials while building a strong foundation in statistical programming, data standards, and regulatory compliance.
This position is ideal for recent graduates in Mathematics, Statistics, or related quantitative disciplines who are enthusiastic about combining analytical skills with programming in a healthcare and clinical research setting.
Key Responsibilities
Support the creation and delivery of derived and CDISC-compliant datasets for clinical trials.
Assist in generating statistical outputs such as tables, listings, and figures for clinical study reporting.
Review and validate AI-generated statistical documents for consistency and compliance with protocols.
Apply SAS programming and other statistical tools to real-world clinical trial projects.
Collaborate with cross-functional teams, including statisticians, data managers, and project managers.
Maintain documentation of work processes and outputs in alignment with industry standards.
Required Qualifications
Bachelor’s or Master’s degree in Statistics, Mathematics, or a related quantitative discipline with strong statistical coursework.
Strong understanding of statistical principles and their application to clinical trials.
Exposure to any programming discipline (SAS, R, Python, or similar).
Excellent PC literacy including Microsoft Office, Teams, and virtual conferencing tools.
Strong analytical, problem-solving, organizational, and communication skills.
Preferred Qualifications
Relevant internship or project experience in pharmaceutical, biotechnology, or CRO environments.
Familiarity with clinical trial processes, regulatory standards (ICH/GCP), and global data standards (CDISC).
Why Join Quanticate?
Quanticate is a world-leading data-focused CRO, delivering advanced statistical programming and data management solutions to top pharmaceutical companies and emerging biotech organizations. By joining Quanticate, you will:
Work on cutting-edge clinical programs and collaborate with global teams.
Gain exposure to CDISC data standards, clinical trial analytics, and regulatory compliance.
Participate in structured professional development including mentoring, coaching, e-learning, and job shadowing.
Receive membership opportunities in professional societies and engage in industry committees.
Contribute to clinical therapies that impact patient outcomes worldwide.
Benefits & Perks
Competitive salary package.
Six-month intensive training program for professional growth.
Flexible working hours and supportive work environment.
Paid holidays, including annual, casual, sick leave, and bank holidays.
Medical insurance coverage for employees and immediate family.
Gratuity and accidental coverage.
Opportunities for learning and skill development including mentoring, coaching, e-learning, and on-the-job training.
How to Apply
Qualified candidates will be considered on merit-based evaluation. Quanticate does not require payments or any paid courses for recruitment. Legitimate correspondence will only come from @quanticate.com email addresses.
Apply via Email: careers@quanticate.com
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