Novotech is inviting applications for the position of Clinical Data Programmer SAS II (CDPSAS) in Bangalore, Karnataka. This full-time opportunity is intended for professionals with experience in SAS programming, clinical data analytics, statistical programming, or business intelligence within the pharmaceutical, clinical research, or EDC software industry.
The role focuses on developing and maintaining analytical solutions that help clinical research teams review study data, monitor clinical site performance, identify data quality issues, and make informed decisions. Responsibilities include creating dashboards, reports, tables, visualizations, and reusable programming solutions for clinical data management and study operations.
Candidates with at least two years of relevant experience, practical SAS skills, and knowledge of clinical trial data may find this opportunity suitable.
Novotech Recruitment 2026: Job Highlights
| Particulars | Details |
|---|---|
| Company | Novotech |
| Job Title | Clinical Data Programmer SAS II |
| Abbreviation | CDPSAS |
| Job Identification | 4366 |
| Job Location | Helios Business Park, Bangalore, Karnataka |
| Employment Type | Full-time |
| Qualification | Graduate degree in a relevant discipline |
| Experience | Minimum 2 years of relevant experience |
| Key Technical Skill | SAS programming |
| Additional Tools | Spotfire, Power BI, SQL, Python, R, and clinical analytics platforms |
| Industry | Clinical Research / Contract Research Organization |
| Salary | Not specified in the supplied job description |
| Application Mode | Online through the company’s careers portal |
About Novotech
Novotech is a global full-service Contract Research Organization (CRO) that provides clinical research and scientific advisory services to the biotechnology and pharmaceutical industries.
Founded in 1997, the company operates across multiple international markets and supports clinical development programmes through its research, regulatory, and operational expertise. Its teams work with clinical research sponsors to help advance the development of treatments and therapies.
Job Description: Clinical Data Programmer SAS II
The Clinical Data Programmer SAS II will develop, validate, deploy, and maintain analytical tools used to review clinical study data and monitor operational performance.
The role involves working closely with Clinical Data Managers, Clinical Data Reviewers, Project Managers, and other study stakeholders. The selected candidate will translate business and study requirements into practical analytical solutions that support data quality, clinical review, risk-based quality management, and efficient study delivery.
The position also requires maintaining validated programs, documenting testing activities, following company procedures, and contributing to technical standards and process improvements.
Key Responsibilities
1. Clinical Study Data Programming
- Work with clinical study teams to understand data requirements and recommend appropriate reports, dashboards, graphs, tables, and listings.
- Manage assigned programming activities from requirements gathering and specification through development, testing, deployment, and maintenance.
- Extract, integrate, transform, and analyze clinical, laboratory, external, and operational datasets.
- Develop reusable programs and analytical outputs to support clinical data inspection, reconciliation, and medical review.
- Help study teams make timely decisions using reliable analytical information.
2. Clinical Data Visualization and Reporting
- Create and maintain dashboards, visualizations, and reports for clinical data management and project teams.
- Develop analytical solutions to monitor clinical site performance and identify unusual data trends.
- Present findings and analytical outputs to relevant stakeholders.
- Conduct review sessions and provide guidance to users on the effective use of reporting tools.
- Support training activities related to developed analytical solutions.
3. Risk-Based Quality Management
- Develop and maintain analytics supporting Risk-Based Quality Management (RBQM) and centralized monitoring.
- Support the monitoring of Key Risk Indicators (KRIs) and Quality Tolerance Limits (QTLs).
- Identify meaningful data trends, potential quality signals, and operational concerns.
- Help clinical teams evaluate site performance and data quality issues.
- Contribute to risk monitoring and study oversight activities.
4. Programming Quality Control and Validation
- Perform quality control, peer review, and troubleshooting of programming deliverables.
- Validate programs and outputs across development, user acceptance testing, and production environments.
- Maintain appropriate test evidence and supporting documentation.
- Follow established validation procedures and data integrity standards.
- Ensure deliverables are accurate, consistent, and suitable for their intended use.
5. Software Tools and Automation
- Maintain proficiency in SAS and relevant clinical analytics technologies.
- Apply tools such as Power BI, TIBCO Spotfire, SQL, Python, R, Medidata Clinical Data Studio, and CluePoints where appropriate.
- Develop reusable templates, macros, standard programs, and automated workflows.
- Contribute validated programs and outputs to controlled, searchable libraries.
- Evaluate suitable technologies to improve quality, scalability, and delivery efficiency.
6. Documentation and Team Collaboration
- Maintain accurate, complete, and inspection-ready project documentation.
- Follow Novotech standard operating procedures and applicable regulatory requirements.
- Participate in Clinical Data Visualization team and Biometrics department meetings.
- Share technical knowledge and support the development of less-experienced colleagues.
- Complete assigned administrative activities and timesheets on time.
- Contribute to improvements in procedures, templates, technical standards, and quality control practices.
Eligibility Criteria
Educational Qualification
Candidates should have a graduate qualification in one of the following areas or a related discipline:
- Computer Science.
- Data Science.
- Mathematics.
- Life Sciences.
- Other relevant fields.
Experience Required
A minimum of two years of relevant experience is required in areas such as:
- Statistical programming.
- Business intelligence.
- Data analysis.
- Data science.
The experience should be within a pharmaceutical company, CRO, or EDC software provider. Practical experience using SAS and/or business intelligence tools to analyze clinical, laboratory, or operational data is required.
Required Technical Skills
Candidates should have practical knowledge of the following:
- SAS programming.
- Clinical study data structures.
- EDC database schemas.
- Clinical data review and reporting processes.
- Data extraction, integration, transformation, analysis, and presentation.
- Data quality control and validation.
- Clinical analytics and visualization tools.
- SOP compliance and documentation practices.
Preferred Skills
The following skills and technologies may be advantageous:
- SQL, Python, or R.
- TIBCO Spotfire, Power BI, Tableau, or Qlik.
- Medidata Clinical Data Studio.
- CluePoints and centralized monitoring platforms.
- Risk-Based Quality Management.
- JReview and clinical data review tools.
- Power Automate or other workflow automation technologies.
- Requirements gathering and stakeholder communication.
- Reusable macros, programs, and reporting templates.
Job Location
The position is based at:
Novotech
Ground Floor, Unit 1, Block E, Helios Business Park,
Bangalore, Karnataka – 560103, India.
The vacancy is listed as a full-time position. The supplied job description does not specify a remote or hybrid arrangement, so candidates should confirm the applicable work setup with the recruitment team.
Salary and Benefits
The salary range has not been disclosed in the supplied job description.
Novotech describes a range of employee support and development initiatives, which may include:
- Flexible working options.
- Paid parental leave for both parents.
- Flexible leave entitlements.
- Wellness programmes.
- Professional development and mentorship.
- Opportunities to work with global clinical research teams.
- Flexible benefits through its NovoLife framework.
The specific benefits applicable to this role may depend on employment terms and location.
How to Apply for Novotech Recruitment 2026
Interested and eligible candidates can apply through Novotech’s official careers portal. Search for the position using the job identification number 4366 or the title Clinical Data Programmer SAS II.
Before submitting your application, prepare an updated resume highlighting your SAS programming experience, clinical data analytics work, reporting tools, data validation skills, and exposure to clinical trials.
Ensure that your resume clearly describes the analytical solutions, dashboards, reports, or programming deliverables you have handled.
Frequently Asked Questions (FAQs)
1. Which company is hiring for Clinical Data Programmer SAS II?
Novotech is recruiting for the Clinical Data Programmer SAS II position.
2. Where is the job located?
The position is based at Helios Business Park in Bangalore, Karnataka.
3. What is the job identification number?
The job identification number is 4366.
4. What qualification is required?
A graduate qualification in Computer Science, Data Science, Mathematics, Life Sciences, or a related field is required.
5. How much experience is needed?
The position requires a minimum of two years of relevant experience in statistical programming, business intelligence, data analysis, or data science.
6. Is SAS programming experience required?
Yes. Practical experience with SAS and/or business intelligence tools for analyzing clinical, laboratory, or operational datasets is required.
7. Which additional tools may be useful?
SQL, Python, R, Power BI, Spotfire, CluePoints, Medidata Clinical Data Studio, and workflow automation tools may be useful for the role.
8. What are the main responsibilities?
The role includes clinical data programming, dashboard development, data visualization, quality control, validation, centralized monitoring analytics, and reporting.
9. What is the salary for this position?
The salary has not been specified in the supplied job description.
10. How can candidates apply?
Candidates can search for job identification number 4366 or the exact job title on Novotech’s official careers portal.
Disclaimer
This article is a rewritten summary of the supplied Novotech job description. Vacancy status, eligibility requirements, compensation, benefits, and work arrangements may change. Candidates should verify the latest information through Novotech’s official recruitment portal before applying.