Clario, part of Thermo Fisher Scientific, has announced recruitment for the position of Statistical Programmer in Bangalore and Remote (India). This opportunity is ideal for professionals with experience in SAS Programming, CDISC, SDTM, ADaM datasets, and clinical trial programming who are looking to advance their careers in the pharmaceutical and clinical research industry.
The role focuses on developing regulatory-compliant clinical datasets, supporting cardiac safety studies, and delivering high-quality statistical programming for global clinical trials.
Job Overview
| Particular | Details |
|---|---|
| Company | Clario (Part of Thermo Fisher Scientific) |
| Position | Statistical Programmer |
| Job Type | Full-Time |
| Location | Bangalore, India / Remote (India) |
| Experience | Bachelor’s + 3 years OR Master’s + 0โ1 year |
| Industry | Clinical Research / Biostatistics |
| Department | Cardiac Solutions |
| Application Mode | Online |
Key Responsibilities
The selected candidate will:
- Develop and maintain CDISC-compliant datasets.
- Create SDTM ECG (EG) and ADaM ADEG datasets.
- Write and validate SAS programs.
- Perform double programming and validation activities.
- Generate compliance checks for CDISC datasets.
- Support statistical analyses for cardiac safety studies.
- Prepare regulatory submission packages.
- Develop Define.xml and reviewer guides.
- Maintain project timelines and deliverables.
- Collaborate with statisticians and cross-functional teams.
- Train team members on programming standards.
- Improve programming processes and quality.
- Support SOPs, SWIs, templates, and documentation.
- Participate in knowledge sharing and onboarding activities.
Required Qualifications
Candidates should possess:
- Bachelor’s degree in Statistics, Mathematics, Computer Science, Biostatistics, or related quantitative discipline with 3+ years of relevant experience
OR
- Master’s degree in a quantitative discipline with 0โ1 year of relevant experience.
Preferred experience includes:
- Pharmaceutical company or CRO experience
- SAS Programming
- CDISC Standards
- SDTM
- ADaM
- Clinical trial programming
- Statistical Analysis Plans (SAP)
- Regulatory submissions
- Clinical data validation
- Microsoft Office
Required Skills
- SAS Programming
- CDISC
- SDTM
- ADaM
- Clinical Trial Data
- Statistical Programming
- Data Validation
- Define.xml
- FDA Submission
- Clinical Research
- Biostatistics
- Regulatory Documentation
- Analytical Skills
- Communication Skills
- Project Management
Employee Benefits
Clario offers:
- Competitive salary
- Performance incentives
- Provident Fund
- Medical Insurance
- Remote work flexibility
- Modern office facilities
- Employee engagement programs
- Learning and development opportunities
- Global clinical research exposure
- Career growth within Thermo Fisher Scientific
Why Join Clario?
Working at Clario allows professionals to contribute to global clinical trials that accelerate the development of life-changing therapies. Employees gain experience with regulatory submissions, cardiac safety studies, advanced SAS programming, and international clinical research standards while collaborating with global teams.
How to Apply
