Argus Safety Tutorial for Beginners: Complete Guide to Oracle Argus Safety in Pharmacovigilance (Argus Safety Tutorial for Beginners) Introduction Argus Safety is one of the most widely used Pharmacovigilance software platforms in the global pharmaceutical industry. Almost every major pharmaceutical company, biotechnology organization, Contract Research Organization (CRO), and drug safety service provider relies on Oracle Argus Safety to manage adverse event reporting, Individual Case Safety Reports (ICSRs), regulatory submissions, and safety surveillance activities. For pharmacy, life sciences, nursing, biotechnology, and healthcare graduates planning a career in Pharmacovigilance, learning Argus Safety can significantly improve employability and career growth opportunities. In this comprehensive Argus Safety tutorial, you will learn the fundamentals of Oracle Argus Safety, its modules, workflow, case processing activities, regulatory reporting functions, and practical application...
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Statistical Programmer Job 2026 in Ahmedabad | SAS & CDISC Jobs at Veeda CR
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Statistical Programmer Job 2026 in Ahmedabad | SAS & CDISC Jobs at Veeda CR
(Statistical Programmer Job 2026 in Ahmedabad)
Introduction
If you are planning to build a career in clinical data science, SAS programming, or biostatistics, this Statistical Programmer job at Veeda Clinical Research (Veeda CR) in Ahmedabad is an excellent opportunity. With the increasing demand for professionals skilled in clinical data management and regulatory standards, this role provides a strong foundation in pharmaceutical data science and clinical research.
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Veeda Clinical Research (Veeda CR) is a well-established Clinical Research Organization (CRO) headquartered in Ahmedabad, India. Founded in 2004, the company has built a strong reputation in bioequivalence studies, clinical trials, and data management services. Veeda operates globally and provides services to pharmaceutical, biotechnology, and generic drug companies. With hundreds of employees and modern research facilities, Veeda CR is known for delivering high-quality clinical data and regulatory compliance solutions.
Job Overview Summary
The Statistical Programmer role at Veeda CR focuses on handling clinical trial data and ensuring it meets global regulatory standards like CDISC and FDA requirements. This role is ideal for candidates with 1–3 years of experience in SAS programming and clinical data analysis, offering exposure to real-world datasets and industry tools.
Vacancy Details (Official)
Company Name: Veeda Clinical Research (Veeda CR)
Role: Statistical Programmer
Location: Ahmedabad, India
Experience: 1–3 Years
Salary: ₹4,00,000 – ₹6,50,000 per annum
Job Type: Full-time, Permanent
Openings: 1
Posted On: April 10, 2026
Responsibility Explanation
As a Statistical Programmer, your primary responsibility will be to manage and analyze clinical trial data using SAS programming. You will work on preparing datasets that comply with CDISC standards such as SDTM and ADaM.
You will also create annotated case report forms (aCRF), develop mapping specifications, and generate metadata files like Define.xml. Running validation checks using Pinnacle 21 and resolving data issues will be part of your daily work.
In addition, you will prepare regulatory documents such as cSDRG and ADRG reports and ensure all data submissions meet FDA guidelines. Automation using SAS macros and maintaining data quality through validation checks are also key responsibilities.
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B.Pharm / M.Pharm / Pharm.D / Life Sciences / Biostatistics
1–3 years of experience in SAS programming or clinical data
Skills Required
Candidates should have strong technical skills in SAS programming and a good understanding of clinical data workflows. Knowledge of CDISC standards such as SDTM and ADaM is essential.
Familiarity with tools like Pinnacle 21 Validator and experience in generating Define.xml files will be beneficial. Analytical thinking, attention to detail, and problem-solving skills are important for handling complex datasets. Good communication skills are also required to work with cross-functional teams.
Salary Estimate
The salary for this role ranges between ₹4 LPA and ₹6.5 LPA. Candidates with strong SAS and CDISC experience may receive higher packages. This field also offers long-term growth, where experienced professionals can earn ₹10 LPA+ in future roles like Senior Statistical Programmer or Biostatistician.
Interview Details (Official Style)
Interview Mode: Virtual / In-person
Rounds:
Technical Round (SAS, CDISC, Clinical Data)
Practical Assessment (Programming Test)
HR Round
Shortlisted candidates will be contacted by HR
Required Documents
Updated Resume (ATS-friendly)
Educational Certificates
Experience Certificates
ID Proof (Aadhar / PAN)
Passport Size Photograph
Any SAS or Clinical Data Certifications
How to Apply (Clean Method)
Interested candidates can apply through the official job link:
Q1. What is the role of a Statistical Programmer? A Statistical Programmer works on clinical trial data using SAS and prepares datasets for regulatory submission.
Q2. What skills are required for this job? SAS programming, CDISC standards, and clinical data analysis skills are required.
Q3. Is this job suitable for freshers? No, candidates need at least 1–3 years of experience.
Q4. What is CDISC? CDISC is a global standard for clinical data used in regulatory submissions.
Q5. What is the salary range? The salary ranges from ₹4 LPA to ₹6.5 LPA.
Final Conclusion
The Statistical Programmer role at Veeda Clinical Research is a great opportunity for candidates looking to build a career in clinical data science and biostatistics. With exposure to global regulatory standards, real-world clinical datasets, and advanced tools, this job offers strong career growth in the pharmaceutical and CRO industry. Candidates with SAS and CDISC knowledge should definitely apply for this opportunity.
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