CPVIA Hiring Statistical Programmers, Biostatisticians & Clinical SAS Programmers | Multiple Openings in Hyderabad

📢 Latest Clinical SAS, Biostatistics & Statistical Programming Jobs 2026

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CPVIA Hiring Statistical Programmers, Biostatisticians & Clinical SAS Programmers | Multiple Openings in Hyderabad | SAS Programming Jobs 2026

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CPVIA Hiring Statistical Programmers, Biostatisticians & Clinical SAS Programmers | Multiple Openings | Hyderabad

🏢 CPVIA

📍 Hyderabad

📊 Statistical Programming

📈 Biostatistics

💻 Clinical SAS

CPVIA is hiring across multiple Clinical Programming and Biostatistics functions including Statistical Programmer, Biostatistician, and Clinical SAS Programmer roles. These openings are suitable for professionals ranging from entry-level candidates to senior and principal-level experts.

Professionals with expertise in SAS Programming, ADaM, TFLs, CDISC, Oncology Studies, Statistical Analysis, Clinical Data Management, and Regulatory Submissions are encouraged to apply.

📋 Recruitment Overview

Particulars	Details
Company	CPVIA
Location	Hyderabad
Experience	0–12+ Years
Industry	Clinical Research / CRO / Biostatistics
Application Mode	Email Application
Email ID	careers@cpvia.com

📊 Statistical Programmer (Junior / Senior / Principal)

Details	Information
Role	Statistical Programmer
Levels	Junior / Senior / Principal
Experience	0–12+ Years
Salary	₹6 – ₹40 LPA

📌 Key Responsibilities

Develop and validate ADaM datasets.
Create Tables, Listings and Figures (TFLs).
Support clinical trial reporting activities.
Perform programming validation.
Ensure CDISC compliance.
Collaborate with Biostatistics teams.
Support regulatory submissions.
Maintain programming documentation.

🎓 Qualification

B.Pharm / M.Pharm
Biostatistics
Statistics
Mathematics
Bioinformatics
Life Sciences
Computer Science

📈 Biostatistician (Junior / Senior)

Details	Information
Role	Biostatistician
Levels	Junior / Senior
Experience	0–7+ Years
Salary	₹8 – ₹20 LPA

📌 Key Responsibilities

Create Statistical Analysis Plans (SAPs).
Perform statistical analyses.
Support protocol design activities.
Perform sample size calculations.
Interpret clinical trial results.
Generate statistical reports.
Work closely with Statistical Programmers.
Support regulatory submissions.

🎓 Qualification

Statistics
Biostatistics
Mathematics
Life Sciences
Pharmacy
Biotechnology

💻 Clinical SAS Programmer

Details	Information
Role	Clinical SAS Programmer
Experience	1–5+ Years
Salary	₹6 – ₹18 LPA

📌 Key Responsibilities

Create DM, MM and Laboratory Listings.
Develop Edit Checks.
Perform Data Reconciliation.
Create Patient Profiles.
Generate Clinical Reports.
Support Clinical Database Review.
Validate SAS Programs.
Support submission activities.

🎓 Qualification

Life Sciences
Pharmacy
Biotechnology
Computer Science
Statistics
Bioinformatics

⭐ Required Skills

Clinical SAS Programming
ADaM Dataset Development
TFL Programming
CDISC Standards
Clinical Trial Data Analysis
Statistical Programming
Clinical Data Management
Excellent English Communication
Problem Solving Skills
Analytical Thinking

🌟 Preferred Skills

ISS (Integrated Summary of Safety)
ISE (Integrated Summary of Efficacy)
Real World Data (RWD)
Real World Evidence (RWE)
R Programming
Oncology Studies
Submission Experience
Leadership Experience

💰 Salary Information

Based on current Clinical Research, CRO, Biostatistics, and Statistical Programming market trends in India, the expected salary ranges are:

Position	Estimated Salary
Junior Statistical Programmer	₹6 – ₹10 LPA
Senior Statistical Programmer	₹12 – ₹22 LPA
Principal Statistical Programmer	₹25 – ₹40 LPA
Biostatistician	₹8 – ₹20 LPA
Clinical SAS Programmer	₹6 – ₹18 LPA

💰 Actual compensation may vary depending on experience, project exposure, therapeutic area expertise, programming skills, and interview performance.

🚀 Why Join CPVIA?

Work on global clinical development programs.
Exposure to Oncology and multiple therapeutic areas.
Opportunity to work on advanced SAS and R Programming projects.
Hands-on involvement in CDISC SDTM and ADaM standards.
Exposure to regulatory submissions and statistical reporting.
Career growth opportunities across Clinical Programming and Biostatistics functions.
Professional and collaborative work environment.
Opportunity to work with experienced statisticians and clinical programmers.
Exposure to Real-World Evidence (RWE) and Real-World Data (RWD) projects.
Long-term career development in the pharmaceutical and CRO industry.

📈 Career Scope After Joining CPVIA

Professionals joining CPVIA can build long-term careers in:

Clinical SAS Programming
Statistical Programming
Biostatistics
Clinical Data Science
Clinical Data Management
Regulatory Submission Programming
Oncology Programming
Real World Evidence Analytics
Healthcare Data Analytics
Clinical Trial Reporting

📄 ATS-Friendly Resume Tips

Use Relevant Keywords: Include keywords such as SAS Programming, Clinical SAS, CDISC, SDTM, ADaM, TFLs, Biostatistics, Oncology, Clinical Trials, R Programming, ISS, and ISE.
Highlight Technical Skills: Clearly mention SAS, SQL, R Programming, Statistical Analysis, Data Validation, and Reporting tools.
Show Project Experience: Mention clinical studies, therapeutic areas, submission work, and programming deliverables.
Add Regulatory Knowledge: Highlight experience with CDISC standards, FDA submissions, and clinical trial reporting.
Quantify Achievements: Mention study sizes, datasets handled, validation activities, and reporting responsibilities wherever possible.

💡 Interview Preparation Tips

Revise SDTM and ADaM concepts thoroughly.
Prepare SAS programming examples and validation scenarios.
Review TFL creation and QC methodologies.
Understand Oncology trial workflows and terminology.
Practice statistical concepts and SAP discussions.
Revise ISS and ISE concepts if applicable.
Be prepared to discuss project challenges and solutions.
Review R Programming basics if mentioned in your profile.
Understand clinical trial phases and drug development lifecycle.
Prepare examples demonstrating teamwork and stakeholder management.

📝 How to Apply

Update your latest resume.
Highlight SAS, ADaM, CDISC, SDTM, TFL, Oncology, and R Programming experience.
Mention therapeutic area expertise if applicable.
Clearly describe submission and validation experience.
Include project accomplishments and key achievements.
Mention the position title in the email subject line.

🚀 Apply Now

📧 Email Resume To:

careers@cpvia.com

📌 Important Application Note:

Mention the position title (Statistical Programmer, Biostatistician, or Clinical SAS Programmer) in the email subject line for faster screening and processing.