Emmes Group is hiring for the position of Senior Statistical Programmer – Contractor in Bengaluru, India. The role is part of the Biometrics/Biostatistics function and is offered on a contract basis.
The Senior Statistical Programmer will be responsible for developing, validating and delivering statistical datasets and outputs used in clinical trial analysis and regulatory submissions. The position requires strong expertise in SAS programming, CDISC standards, SDTM and ADaM, along with experience working in a pharmaceutical, biotechnology or CRO environment.
Candidates with a Bachelor’s degree in Computer Science, Statistics, Mathematics, Life Sciences or a related discipline and 4–6 years of statistical programming experience may be eligible for this opportunity.
Emmes Group Senior Statistical Programmer – Job Highlights
| Particular | Details |
|---|---|
| Company | Emmes Group |
| Job Title | Senior Statistical Programmer |
| Employment Type | Contract |
| Location | Bengaluru, India |
| Department | Biometrics / Biostatistics |
| Experience | 4–6 Years |
| Qualification | Bachelor’s degree required; Master’s preferred |
| Key Skills | SAS, SQL, SAS Macro, CDISC, SDTM, ADaM |
| Clinical Phase | Phase I–IV |
| Job ID | 3448 |
| Salary / CTC | Not specified |
About Emmes Group
Emmes Group is a clinical research and technology organization working across areas including clinical research, data, analytics and technology. The organization operates through its business units, including Emmes, a full-service CRO, and Veridix AI, which focuses on technology, data and analytical solutions.
Its research experience includes areas such as cell and gene therapy, vaccines, infectious diseases, ophthalmology, rare diseases and neuroscience.
Job Description
The Senior Statistical Programmer will support clinical research programs by creating and validating statistical datasets, tables, listings and figures required for clinical analysis and regulatory submissions.
The position works closely with Biostatistics, Clinical Data Management, Clinical and Regulatory teams to ensure that programming deliverables meet clinical study requirements, applicable standards and project timelines.
The role requires practical experience with SAS programming and CDISC-compliant clinical data standards, particularly SDTM and ADaM.
Senior Statistical Programmer – Role Overview
The selected candidate will contribute to statistical programming activities across Phase I to Phase IV clinical trials.
Key areas of responsibility include:
- Clinical trial statistical programming
- SDTM and ADaM dataset development
- Tables, Listings and Figures (TLFs)
- Clinical Study Report (CSR) support
- Statistical Analysis Plan implementation
- Programming validation
- Regulatory submission support
- Programming documentation
- Quality control
- Process and standards improvement
Educational Qualification
Required
Candidates should have a Bachelor’s degree in one of the following or a related field:
- Computer Science
- Statistics
- Mathematics
- Life Sciences
- Related discipline
Preferred
A Master’s degree in Computer Science, Statistics, Mathematics, Life Sciences or a related field is preferred.
Experience Requirements
Candidates should have:
- 4–6 years of experience as a statistical programmer.
- Experience in a pharmaceutical, biotechnology or CRO environment.
- Experience supporting clinical trial reporting and statistical programming activities.
- Experience preparing clinical data and outputs for regulatory submissions is highly relevant.
Technical Skills
The position requires strong programming capabilities in:
- SAS Base
- SAS Macro
- SAS SQL
- Clinical trial statistical programming
- CDISC standards
- SDTM
- ADaM
- Tables, Listings and Figures (TLFs)
- Statistical Analysis Plans (SAPs)
Knowledge of R or Python is an additional advantage.
Regulatory and Clinical Research Knowledge
Candidates should have a strong understanding of clinical research programming requirements, including:
- Clinical trial reporting
- Regulatory submission preparation
- CDISC standards
- SDTM datasets
- ADaM datasets
- Good Clinical Practice (GCP)
- ICH requirements
- 21 CFR Part 11
- Regulatory expectations of agencies such as the FDA and EMA
Key Responsibilities
Statistical Programming and Dataset Development
The Senior Statistical Programmer will:
- Develop SDTM datasets according to applicable CDISC standards.
- Create and program ADaM datasets for clinical analysis.
- Develop Tables, Listings and Figures for clinical study reporting.
- Translate Statistical Analysis Plans into reliable and efficient programming code.
- Test and validate statistical programming outputs.
- Prepare programming deliverables required for clinical trial analysis and regulatory activities.
Study and Project Support
Responsibilities also include:
- Serve as the lead programmer for assigned clinical studies or studies within a broader program.
- Coordinate with Biostatisticians, Clinical Data Managers and Regulatory teams.
- Understand study requirements and deliver programming outputs according to project timelines.
- Support clinical teams with accurate and timely statistical programming deliverables.
Quality and Compliance
The role will involve:
- Performing independent quality checks of programming outputs.
- Reviewing datasets and statistical results for accuracy and consistency.
- Maintaining appropriate programming documentation.
- Following internal Standard Operating Procedures.
- Ensuring programming activities align with relevant regulatory requirements.
- Working in accordance with GCP, ICH and 21 CFR Part 11 expectations.
Process Improvement
The selected candidate may also contribute to:
- Development and improvement of programming standards.
- Creation and refinement of reusable SAS macros.
- Development of reusable programming code libraries.
- Identification of opportunities to improve programming workflows.
- Process optimization and efficiency improvements within the statistical programming team.
Other duties may be assigned according to business and project requirements.
Required Professional Skills
Candidates should demonstrate:
- Strong attention to detail
- Analytical and problem-solving ability
- Effective written and verbal communication
- Ability to work independently
- Ability to collaborate with cross-functional teams
- Strong clinical programming knowledge
- Ability to work effectively in a fast-paced environment
- Commitment to quality and regulatory compliance
Work Location and Employment Type
- Job Location: Bengaluru, India
- Employment Type: Contract
- Department: Biometrics / Biostatistics
- Job ID: 3448
The available vacancy information does not specify a remote or hybrid work arrangement.
Salary / CTC
The salary or contract compensation for the Senior Statistical Programmer position has not been specified in the available job information.
Candidates should confirm compensation and contract-related terms directly through the employer’s recruitment process.
Selection Process
The detailed selection process has not been specified in the provided vacancy information.
Candidates are likely to be assessed based on their statistical programming experience, SAS proficiency, CDISC knowledge, clinical trial experience, regulatory understanding and ability to work with cross-functional teams.
How to Apply
Interested candidates should apply through the official Emmes Group careers platform and review the complete vacancy requirements before submitting their application.
Candidates should ensure that their resume clearly highlights experience with SAS, SDTM, ADaM, CDISC, TLF programming and clinical trial reporting where applicable.
Important Details Before Applying
- The position is based in Bengaluru, India.
- This is a contract position.
- The department is Biometrics/Biostatistics.
- Candidates should have 4–6 years of statistical programming experience.
- A Bachelor’s degree in a relevant discipline is required.
- A Master’s degree is preferred.
- Strong SAS Base, Macro and SQL skills are expected.
- Strong knowledge of CDISC SDTM and ADaM is required.
- Clinical trial reporting and regulatory submission experience is highly relevant.
- Knowledge of R or Python is an advantage.
- The job ID is 3448.
- Salary/CTC has not been disclosed in the available vacancy information.
Frequently Asked Questions
1. What is the job title?
The position is Senior Statistical Programmer – Contractor.
2. Which company is hiring?
The vacancy is with Emmes Group.
3. Where is the job located?
The position is based in Bengaluru, India.
4. What is the employment type?
The position is offered on a contract basis.
5. How much experience is required?
The vacancy requires 4–6 years of experience as a statistical programmer in a pharmaceutical, biotechnology or CRO environment.
6. What qualification is required?
A Bachelor’s degree in Computer Science, Statistics, Mathematics, Life Sciences or a related discipline is required. A Master’s degree is preferred.
7. Is SAS knowledge required?
Yes. Strong programming skills in SAS Base, SAS Macro and SQL are required for this position.
8. Is CDISC knowledge required?
Yes. In-depth knowledge of CDISC SDTM and ADaM standards is an important requirement.
9. Is clinical trial experience required?
The role requires experience supporting clinical trial reporting and preparing data for regulatory submissions.
10. Is knowledge of R or Python required?
R or Python is listed as a plus, so it can be an additional advantage.
11. Which regulatory standards are relevant?
The role requires compliance with standards and requirements including GCP, ICH and 21 CFR Part 11.
12. What is the salary for this position?
The salary or contract compensation has not been specified in the available vacancy details.
13. What is the job ID?
The job ID is 3448.
Important Note
Job availability, eligibility requirements, contract conditions, compensation and other recruitment details may change. Candidates should verify the latest vacancy information and complete application requirements through the employer’s official recruitment channel before applying.