IQVIA is hiring for the position of Clinical Data Management SAS Programmer for candidates with experience in SAS programming, clinical data management, and the pharmaceutical or healthcare industry. The opportunity is listed as a full-time role, with Bangalore and Kochi mentioned as locations and a hybrid work arrangement.
This position is suitable for professionals with experience in clinical SAS programming, SQL, SAS macros, clinical data processing, and report generation. The role involves creating clinical datasets, preparing listings and customised reports, importing raw data, and supporting the preparation and delivery of clinical data to clients.
According to the supplied official job listing, candidates should have 2–10 years of relevant work experience, with at least two years of programming experience specified in the qualifications section. The application deadline is listed as October 30, 2026.
IQVIA Recruitment 2026: Job Highlights
| Particulars | Details |
|---|---|
| Company | IQVIA |
| Job Title | Clinical Data Management SAS Programmer |
| Job Requisition ID | R1569129 |
| Job Locations | Bangalore and Kochi, India |
| Work Location Requirement | Any location in India, as stated in the project details |
| Work Mode | Hybrid |
| Employment Type | Full-time |
| Experience | 2–10 years |
| Required Education | Bachelor’s degree in Computer Science or a related discipline |
| Key Skills | SAS, SQL, Macros, Clinical Data Management |
| Industry | Clinical Research, Pharmaceutical and Healthcare |
| Posting Date | Listed as “Posted Today” in the supplied source |
| Application Deadline | October 30, 2026 |
| Salary | Not disclosed |
| Application Mode | Online |
About IQVIA
IQVIA is a global provider of clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries. The company works with organisations involved in developing and commercialising medical treatments.
Its work combines clinical research, data, technology, and healthcare expertise to support research activities and improve patient outcomes.
Job Description: Clinical Data Management SAS Programmer
The Clinical Data Management SAS Programmer will use SAS programming and related technologies to process clinical data, develop datasets, and generate reports according to project and client requirements.
The role requires an understanding of clinical research processes, clinical trial phases, data structures, and statistical programming techniques. The candidate will work with raw data, create project-specific macros and formats, develop clinical datasets, and prepare data outputs for internal use or client delivery.
Strong technical knowledge of Base SAS, advanced SAS programming, SAS macros, SQL, and SAS Grid is highlighted in the supplied job description.
Key Responsibilities
1. Clinical SAS Programming and Data Processing
- Create SAS datasets from raw clinical data.
- Import and process data from different sources and platforms.
- Read raw data files, build appropriate data structures, and manage missing values.
- Append and concatenate SAS datasets as required.
- Access, organise, and manage clinical data for project needs.
- Create status and efficacy datasets according to project specifications.
2. SAS Reports and Data Listings
- Generate reports using SAS reporting procedures.
- Use procedures such as PROC PRINT, PROC FREQ, PROC MEANS, PROC TRANSPOSE, and PROC SQL.
- Prepare clinical data listings and customised reports according to client requirements.
- Use SAS Output Delivery System (ODS) to produce reports in formats such as RTF, PDF, and HTML.
- Ensure reports are prepared in the required formats and meet project expectations.
3. SAS Macros and SQL
- Develop and use SAS macros for recurring programming tasks.
- Create project-specific macros and formats.
- Use SQL for querying, processing, and managing data.
- Write code using Base SAS programs, SAS procedures, or standardised macros.
- Troubleshoot programming errors and improve the reliability of data-processing workflows.
4. Clinical Data Management
- Apply clinical domain knowledge when processing clinical trial data.
- Understand clinical phases and the data requirements associated with clinical research.
- Prepare datasets and reports that support clinical data management activities.
- Help ensure that clinical data outputs are accurate, organised, and suitable for their intended use.
5. Vendor Data Import and Client Deliverables
- Support vendor import programming.
- Load client data received from other platforms.
- Process imported data according to project requirements.
- Prepare data for delivery to clients.
- Develop listings and reports tailored to customer specifications.
6. Quality and Communication
- Identify and resolve SAS programming errors.
- Follow project coding standards and use standardised macros where applicable.
- Communicate technical issues and project updates effectively.
- Collaborate with colleagues and relevant stakeholders to support project deliverables.
Eligibility Criteria
Educational Qualification
The official job description specifies a Bachelor’s degree in Computer Science or a related discipline as a required qualification.
Candidates should review the official application page to confirm whether their particular educational background meets IQVIA’s requirements.
Work Experience
The supplied project details specify 2–10 years of work experience.
The qualifications section also requires at least two years of applications programming experience, or an alternative pathway involving specialised IT experience that meets the stated Technology Experience Ratio of 25–50%.
Candidates should verify the applicable experience criteria directly on the official vacancy page.
Required Technical Skills
Applicants should have knowledge or experience in the following areas:
- Clinical SAS programming.
- Base SAS and advanced SAS.
- SAS macros.
- SAS SQL and PROC SQL.
- SAS data import programming.
- SAS Output Delivery System (ODS).
- Clinical data processing and dataset creation.
- PROC PRINT, PROC FREQ, PROC MEANS, and PROC TRANSPOSE.
- Data handling, missing values, and data concatenation.
- Clinical trial processes and clinical phases.
- Vendor data import programming.
- SAS Grid.
- Programming troubleshooting and error handling.
Domain Knowledge
Experience in the clinical, pharmaceutical, healthcare, or related clinical research domain is specifically highlighted in the project requirements.
Candidates should understand clinical data management workflows and how SAS programming supports the preparation, processing, and reporting of clinical trial data.
Job Location and Work Mode
The job listing identifies Bangalore and Kochi as locations, while the project details state that the work location can be anywhere in India. The work mode is described as hybrid.
| Work Detail | Information |
|---|---|
| Primary Listed Locations | Bangalore and Kochi |
| Country | India |
| Work Mode | Hybrid |
| Employment Schedule | Full-time |
Because the listing contains multiple location references, applicants should confirm the eligible work location, office attendance requirements, and any relocation expectations with IQVIA during the application process.
Salary and Benefits
The salary for the Clinical Data Management SAS Programmer position has not been disclosed in the supplied job listing.
Specific details about bonuses, insurance, paid leave, or other employee benefits were not included. Candidates can review the official vacancy page or discuss compensation with the employer during recruitment.
How to Apply for IQVIA Recruitment 2026
Interested and eligible candidates can apply through IQVIA’s official Workday recruitment portal.
Application steps:
- Open the official IQVIA application page.
- Confirm the job title: Clinical Data Management SAS Programmer.
- Verify the requisition ID: R1569129.
- Review the educational requirements, experience criteria, and technical skills.
- Complete the online application and submit your updated resume.
Last Date to Apply: October 30, 2026.
Candidates should apply promptly and verify that the vacancy remains open on the official portal.
Frequently Asked Questions (FAQs)
1. What is the job role at IQVIA?
IQVIA is recruiting for the position of Clinical Data Management SAS Programmer.
2. What is the requisition ID?
The job requisition ID is R1569129.
3. Where is the job located?
Bangalore and Kochi are listed as locations. The project details also state that the work location may be anywhere in India.
4. What is the required experience?
The project details specify 2–10 years of work experience, while the qualifications section requires at least two years of applications programming experience or an eligible alternative experience pathway.
5. What qualification is required?
A bachelor’s degree in Computer Science or a related discipline is specified in the supplied job description.
6. Which technical skills are required?
Key skills include Base SAS, advanced SAS, SQL, SAS macros, clinical data processing, data import programming, and SAS report generation.
7. Is clinical or pharmaceutical domain experience required?
Yes. The project details specifically highlight work experience in the clinical, healthcare, or pharmaceutical domain.
8. Is this a remote job?
The position is listed as hybrid, with Bangalore and Kochi as locations. The project details mention any location in India, so candidates should confirm the exact arrangement with IQVIA.
9. What is the salary for this position?
The salary has not been disclosed in the supplied job listing.
10. What is the last date to apply?
The supplied listing states October 30, 2026, as the application deadline.
11. How can I apply?
Candidates can apply through the official IQVIA Workday application page.
Disclaimer
This article is based on the supplied official IQVIA job listing for Clinical Data Management SAS Programmer, requisition R1569129. Job availability, location arrangements, eligibility requirements, and application deadlines may change. Candidates should verify the latest details on IQVIA’s official recruitment portal before applying. Salary and specific benefits were not disclosed in the supplied information.