SAS Programmer Job at Clario Bangalore or remote India with CDISC, SDTM, ADaM, TLF programming and global clinical exposure.
About the Company
Clario is a globally recognized leader in clinical trial endpoint technology, partnering with pharmaceutical, biotechnology, and clinical research organizations to generate high-quality, regulatory-ready clinical evidence. Clario integrates scientific expertise, advanced analytics, and innovative technology to support imaging, cardiac safety, respiratory, and digital endpoint solutions across all phases of clinical development.
With a strong international presence and a mission to unlock better evidence, Clario plays a vital role in accelerating drug development and improving patient outcomes worldwide. The organization fosters a collaborative, inclusive, and performance-driven culture where professionals are encouraged to innovate, learn continuously, and contribute meaningfully to global healthcare advancements. SAS Programmer Job at Clario
Joining Clario means working at the intersection of data, science, and technology while supporting life-changing therapies that reach patients faster and more safely. SAS Programmer Job at Clario
Job Details
- Job Title: SAS Programmer
- Job Requisition ID: R16918
- Employment Type: Full-Time
- Location: Bangalore, India / India Remote
- Work Mode: Hybrid or Remote (India-based candidates)
- Industry: Clinical Research, Biostatistics, Statistical Programming
- Experience Required: Minimum 6 Years
This role is suited for experienced SAS programming professionals who have strong expertise in CDISC standards and are comfortable supporting complex clinical trial data and regulatory submissions. SAS Programmer Job at Clario
Job Description
The SAS Programmer will be responsible for delivering high-quality statistical programming solutions in support of clinical trials across various therapeutic areas. This position focuses on the development, testing, and maintenance of SAS programs for CDISC-compliant datasets, analysis datasets, and regulatory submission deliverables.
The role requires close collaboration with statisticians, data managers, and cross-functional project teams to ensure accurate and timely generation of Tables, Listings, and Figures (TLFs) for Clinical Study Reports. The SAS Programmer will also contribute to electronic submission packages for regulatory authorities, ensuring compliance with global standards and timelines. SAS Programmer Job at Clario
This is a senior-level role offering opportunities to influence processes, mentor team members, and contribute to continuous improvement initiatives within the Statistics and Programming function. SAS Programmer Job at Clario
Key Responsibilities
- Provide end-to-end statistical programming support for assigned clinical studies.
- Develop and review dataset specifications based on study protocols and Statistical Analysis Plans (SAPs).
- Create, test, and maintain SAS programs for analysis datasets, including implementation of analysis-specific flags.
- Generate CDISC-compliant SDTM and ADaM datasets in coordination with internal stakeholders and external clients.
- Ensure datasets meet regulatory standards and internal quality requirements.
- Develop define.xml files and dataset reviewer’s guides for FDA and other regulatory submissions.
- Support statisticians in the preparation of Tables, Listings, and Figures (TLFs) for clinical study reports.
- Perform validation and quality control of programming outputs to ensure accuracy and consistency.
- Provide programming support for ad-hoc analyses and client-specific data requests.
- Participate in and contribute to process improvement initiatives within the Statistics group.
- Recommend enhancements to SOPs and implement improved programming procedures when required.
- Mentor junior programmers and support onboarding and technical skill development within the team.
- Maintain clear, organized, and inspection-ready programming documentation.
- Ensure adherence to SOPs, regulatory guidelines, and industry best practices.
- Collaborate effectively within a matrix organization and across global project teams.
SAS Programmer Job at Clario
Skills / Qualifications
- Bachelor’s or Master’s degree in Statistics, Biostatistics, Mathematics, Life Sciences, or a related discipline.
- Minimum of 6 years of hands-on experience using SAS products and procedures in pharmaceutical or life sciences environments.
- Strong expertise in CDISC standards, including SDTM and ADaM dataset development.
- Proven experience supporting clinical trials and regulatory submissions.
- Solid understanding of pharmaceutical drug development processes and clinical trial methodology.
- Experience generating Tables, Listings, and Figures (TLFs) for Clinical Study Reports.
- Familiarity with define.xml creation and regulatory submission requirements.
- Strong analytical, problem-solving, and attention-to-detail skills.
- Excellent organizational and time management abilities to handle multiple priorities.
- Strong written and verbal communication skills for cross-functional collaboration.
- Ability to work effectively in team-based and matrix organizational structures.
- Proficiency with Windows operating systems and Microsoft Office applications.
- Based in India or able to work remotely from India with flexibility for global collaboration.
SAS Programmer Job at Clario
Benefits / Perks
- Competitive compensation aligned with industry benchmarks.
- Performance-based incentives and recognition programs.
- Provident Fund and comprehensive medical insurance coverage.
- Flexible work arrangements including remote and hybrid models.
- Modern office facilities for employees working on-site.
- Employee engagement initiatives, learning programs, and local events.
- Access to continuous professional development and advanced training.
- Exposure to global clinical trials and high-impact regulatory projects.
- Inclusive, collaborative, and growth-oriented work environment.
SAS Programmer Job at Clario
Why You Should Join
Clario offers a unique opportunity to work on globally impactful clinical research projects while advancing your career in statistical programming. As a SAS Programmer, you will play a critical role in transforming raw clinical data into meaningful, regulatory-ready evidence that supports drug approvals and patient safety. SAS Programmer Job at Clario
The organization values technical excellence, innovation, and teamwork, providing professionals with the resources and flexibility needed to perform at their best. With exposure to international clients, complex clinical studies, and evolving regulatory landscapes, this role offers long-term career growth and professional fulfillment. SAS Programmer Job at Clario
If you are an experienced SAS Programmer seeking challenging work, stability, and the chance to make a real difference in healthcare, Clario is an ideal place to grow. SAS Programmer Job at Clario
FAQs
Who is eligible to apply for this SAS Programmer role?
Professionals with at least 6 years of SAS programming experience in pharma or life sciences and strong CDISC knowledge are eligible.
Is this position available for remote work?
Yes, the role offers remote and hybrid work options for candidates based in India.
Is experience with SDTM and ADaM mandatory?
Yes, hands-on experience with CDISC SDTM and ADaM standards is essential for this role.
Will I work directly with statisticians?
Yes, close collaboration with statisticians for TLF generation and analysis support is a key part of the role.
Does this role include mentoring responsibilities?
Yes, experienced candidates may mentor junior programmers and support team development initiatives.
How to Apply
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