SCL IT Hiring Statistical Programmer II

SAS Programmer Clinical Jobs SCL IT 3-5 Yrs Hiring

SCL IT hiring Statistical Programmer II. SAS, CDISC, SDTM skills required with 3–5 yrs experience in clinical trials.

URL Slug: scl-it-statistical-programmer-sas-clinical

SCL IT Hiring Statistical Programmer II – Clinical SAS & CDISC Roles for 3–5 Years Experience

SCL IT Technologies is hiring for multiple vacancies in the Clinical Data & Biostatistics domain for the position of Statistical Programmer II. This opportunity is designed for professionals with 3 to 5 years of experience in clinical SAS programming, CDISC standards, and clinical trial data analysis.

The role is ideal for candidates who have hands-on experience in Base SAS, SAS Macros, PROC SQL, and have worked on SDTM, ADaM, and TLF development. If you are looking to build a career in clinical research, biostatistics, and pharmaceutical data analytics, this is a strong opportunity to work in a technology-driven pharma environment.

Company Overview

SCL IT Technologies is a growing organization focused on accelerating pharmaceutical innovation through advanced technology solutions, clinical data management, and statistical programming services. The company supports global pharmaceutical and biotechnology clients by delivering high-quality clinical trial data analysis, regulatory-compliant datasets, and reporting solutions.

With expertise in CDISC standards, data standardization, and regulatory submissions, SCL IT plays a critical role in enabling faster drug approvals and ensuring data integrity across clinical studies. The company provides a strong platform for professionals looking to build careers in clinical SAS programming, biostatistics, and regulatory data sciences.

Job Role & Responsibilities

Statistical Programmer II – Clinical SAS Programming

As a Statistical Programmer, you will be responsible for handling clinical trial datasets, developing analysis-ready data, and supporting regulatory submissions using industry-standard programming tools.

Key responsibilities include:

• Develop and validate datasets using CDISC standards such as SDTM and ADaM
• Create Tables, Listings, and Figures (TLFs) for clinical study reports
• Write efficient SAS programs using Base SAS, PROC SQL, and SAS Macros
• Perform data cleaning, validation, and quality checks on clinical trial data
• Collaborate with biostatistics and clinical teams for analysis requirements
• Ensure compliance with regulatory guidelines and data standards
• Maintain documentation for programming activities and validation processes
• Support submission activities for regulatory authorities

This role is crucial in ensuring accurate clinical data analysis, which directly contributes to drug development, regulatory approvals, and patient safety.

Eligibility / Qualifications

Candidates must have completed:

B.Sc, M.Sc, B.Pharm, M.Pharm, Biotechnology, Life Sciences

Relevant courses include: Biostatistics, Clinical Research, Data Science, SAS Programming, Pharmaceutical Sciences, Biotechnology, Bioinformatics, Applied Statistics

• Experience: 3 to 5 years in clinical SAS programming or biostatistics
• Strong knowledge of Base SAS, SAS Macros, and PROC SQL
• Hands-on experience with SDTM, ADaM, and TLF development
• Good understanding of CDISC standards and clinical trial processes
• Experience working with clinical datasets and regulatory submissions preferred

Location & Salary

• Job Location: Not explicitly mentioned (Corporate/Remote/Hybrid depending on company policy)
• Salary: Competitive and aligned with industry standards for clinical SAS programming roles

Application Process

Interested candidates can apply by sending their updated resume to:

Email: vancha.r@sclittechnologies.com

For more information, visit the official website:
https://www.sclittechnologies.com

Ensure your resume highlights your experience in SAS programming, CDISC datasets, and clinical trial data analysis to improve your chances of selection.

Why This Opportunity Stands Out

• Opportunity to work in high-demand clinical SAS programming roles
• Exposure to global clinical trials and regulatory submissions
• Strong career growth in biostatistics and clinical data analytics
• Work on CDISC-compliant datasets and regulatory reporting
• Contribution to drug development and healthcare innovation

FAQs

Who can apply for this role?
Candidates with life sciences, pharmacy, or statistics background and SAS experience can apply.

Is CDISC knowledge mandatory?
Yes, understanding of SDTM and ADaM is important.

What tools are required for this role?
Base SAS, SAS Macros, PROC SQL.

Is prior clinical trial experience required?
Yes, exposure to clinical data is expected.

How to apply?
Send your resume to the provided email ID.

Summary Table

Category	Details
Company	SCL IT Technologies
Vacancies	Statistical Programmer II
Required Education	B.Sc, M.Sc, B.Pharm, M.Pharm, Biotechnology
Experience	3 to 5 Years