Job Title: SAS Programmer
Location: Bangalore, India | Remote (India)
Job Type: Full-Time
Posted: Yesterday
Job Requisition ID: R16918
About Us:
Clario is a global leader in clinical trial endpoint technology, providing innovative solutions that accelerate evidence generation and improve patient outcomes. Our team collaborates with pharmaceutical, biotech, and clinical research organizations to ensure high-quality statistical programming, regulatory compliance, and robust data management.
Role Overview:
We are seeking an experienced SAS Programmer to develop, test, and maintain SAS code for CDISC-compliant datasets, generate Tables, Listings, and Figures (TLFs) for Clinical Study Reports, and support electronic submission packages for regulatory compliance. This role combines statistical programming expertise with collaboration across internal teams and clients.
Key Responsibilities:
Support statistical programming activities for assigned clinical studies.
Develop dataset specifications according to study requirements.
Write, test, and maintain SAS code for analysis datasets, including analysis-specific flags per Statistical Analysis Plan (SAP).
Generate CDISC-compliant SDTM and ADaM datasets in coordination with internal teams and clients.
Prepare define.xml files and dataset reviewer’s guides for FDA submissions.
Assist statisticians in creating TLFs for clinical study reports.
Provide programming support for ad-hoc client requests.
Participate in process improvement initiatives and mentor junior programmers.
Recommend and implement SOPs to improve statistical programming procedures.
Required Skills and Qualifications:
Education: Bachelor’s or Master’s degree in Statistics, Biostatistics, or related field.
Experience: Minimum 6 years of SAS programming experience in pharmaceutical, life sciences, or clinical research settings.
Hands-on experience with CDISC SDTM and ADaM standards.
Understanding of pharmaceutical drug development and clinical trial processes.
Strong analytical, organizational, and communication skills.
Detail-oriented with excellent time management and problem-solving abilities.
Ability to work effectively in teams and within a matrix organization.
Proficiency in Windows and Microsoft Office; experience generating TLFs is a plus.
Based in India or able to work remotely/hybrid from India.
Why Join Clario:
Competitive pay, incentives, and benefits including provident fund and medical insurance.
Flexible remote/hybrid work environment with modern office facilities.
Opportunity to contribute to global clinical trials and regulatory submissions.
Professional growth through mentoring, training, and cross-functional collaboration.
Make a meaningful impact on patient outcomes and the advancement of clinical science.
Learn more at clario.com.
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