Job Overview
| Particulars | Details |
|---|---|
| Position | Intern Statistical Programmer |
| Company | ClinChoice |
| Location | Bengaluru |
| Job Type | Full-Time |
| Experience | Fresher |
| Category / Department | CDM |
| Application Mode | Online |
🏢 About ClinChoice
📝 Job Description
🚀 WE’RE HIRING – Intern Statistical Programmer/Analyst 🚀
Looking to start your career in Clinical Research, SAS Programming, Biostatistics, and Biometrics? 🌍📊
ClinChoice is hiring Freshers for the role of Intern – Statistical Programmer/Analyst in Bengaluru. This is an exciting opportunity for candidates from life sciences, pharmacy, biotechnology, statistics, and data science backgrounds to gain hands-on exposure to real-world clinical trial programming and global CRO workflows.
🏢 Company: ClinChoice
👉 Role: Intern: Statistical Programmer/Analyst
👉 Experience: Freshers
📍 Location: Bengaluru
💼 Department: Statistical Programming / Biometrics
🕘 Employment Type: Full-Time Internship
💰 Expected Salary/Stipend: ₹2.5 LPA – ₹4 LPA (depending on qualifications, skills, and internship structure)
📖 About ClinChoice:
ClinChoice is a global Clinical Research Organization (CRO) established in 1995. The company supports pharmaceutical, biotechnology, medical device, vaccine, and healthcare innovators through services including:
• Clinical Operations
• Biometrics
• Regulatory Affairs
• Pharmacovigilance
• Medical Affairs
• Statistical Programming
• Technology Solutions
ClinChoice operates globally across the United States, Canada, the United Kingdom, China, Japan, India, and several other regions.
🔧 Key Responsibilities:
• Complete clinical programming training programs within timelines
• Learn and apply SAS/R programming concepts
• Develop statistical analysis outputs including:
- Tables
- Listings
- Figures (TLFs)
• Perform programming according to SOPs and specifications
• Work on CDISC SDTM standards
• Collaborate with internal project and study teams
• Report issues and communicate progress effectively
• Participate in knowledge-sharing and process improvement sessions
• Ensure quality-focused delivery of assigned tasks
• Support low-complexity clinical study programming activities
🛠 Required Skills & Qualifications:
🎓 Educational Qualification:
Candidates from the following backgrounds may apply:
• B.Pharm
• M.Pharm
• Biotechnology
• Life Sciences
• Statistics
• Biostatistics
• Data Science
• Computer Science
• Related Healthcare or Scientific disciplines
💡 Preferred Skills:
• Basic knowledge of SAS or R programming
• Understanding of clinical trials and data analysis
• Interest in Clinical Research and Biometrics
• Strong communication skills
• Team collaboration mindset
• Willingness to learn new technologies and standards
🎯 Preferred Competencies:
ClinChoice is looking for candidates who are:
• Quality-focused
• Professional and trustworthy
• Result-driven
• Persistent and accountable
• Good team players
• Able to prioritize tasks effectively
✨ Why Join ClinChoice?
Working at ClinChoice offers exposure to global clinical research projects and real-world statistical programming workflows.
🌟 Benefits of This Internship:
• Industry exposure in Clinical Research
• Hands-on SAS/R programming experience
• Learning opportunity on CDISC standards
• Work with experienced biometrics professionals
• Global CRO work environment
• Career pathway into Statistical Programming and Biostatistics
💬 Join WhatsApp Group: Join Now
⚡ Start your journey in Clinical SAS Programming and Biometrics with a globally recognized CRO and build a strong foundation for a successful clinical research career!
🎯 Key Responsibilities
- ✓ Complete clinical programming training programs within timelines
- ✓ Learn and apply SAS/R programming concepts
- ✓ Develop statistical analysis outputs including:
- ✓ Tables
- ✓ Listings
- ✓ Figures (TLFs)
- ✓ Perform programming according to SOPs and specifications
- ✓ Work on CDISC SDTM standards
- ✓ Collaborate with internal project and study teams
- ✓ Report issues and communicate progress effectively
- ✓ Participate in knowledge-sharing and process improvement sessions
- ✓ Ensure quality-focused delivery of assigned tasks
- ✓ Support low-complexity clinical study programming activities
💡 Required Qualifications & Skills
- ✓ Basic knowledge of SAS or R programming • Understanding of clinical trials and data analysis • Interest in Clinical Research and Biometrics • Strong communication skills • Team collaboration mindset • Willingness to learn new technologies and standards