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Associate Statistical Programmer Job in Bengaluru at Emmes Group

Associate Statistical Programmer Job in Bengaluru at Emmes Group. Apply online for SAS programming and clinical research job opportunity in India.

If you are looking to build a career in biostatistics and clinical data programming, this opportunity offers a strong entry into global clinical research. A leading clinical research organization is hiring Associate Statistical Programmers to support clinical trials and regulatory submissions. This role is ideal for candidates with knowledge of SAS programming and an interest in clinical data analysis.


Company Overview

Emmes Group is a well-established clinical research organization with over four decades of experience in advancing medical research. The company has contributed significantly to areas such as vaccines, infectious diseases, neuroscience, and rare diseases. With a strong presence in global clinical trials and partnerships, Emmes focuses on innovation, data-driven research, and improving patient outcomes worldwide.


Job Overview (Job Details)

CategoryDetails
OrganizationEmmes Group
RoleAssociate Statistical Programmer
QualificationBachelor’s Degree (Scientific Discipline Preferred)
ExperienceEntry-Level / Early Career
Job LocationBengaluru
Employment TypeFull-Time
DepartmentBiometrics / Biostatistics
Application ModeOnline
SalaryNot Disclosed

Job Location & Employment Type

The position is based in Bengaluru and is a full-time role within the biometrics and biostatistics function.


Open Positions / Department Details

The hiring is within the Biometrics / Biostatistics department. The role focuses on statistical programming for clinical trials, including data validation, analysis datasets, and regulatory submissions.


Key Roles & Responsibilities

Selected candidates will be responsible for:

  • Providing statistical programming support for clinical research projects
  • Developing and validating programs using SAS (Base SAS and Macros)
  • Creating analysis datasets and generating tables, listings, and figures (TLFs)
  • Ensuring compliance with CDISC standards and regulatory requirements
  • Supporting clinical trial data analysis and reporting
  • Writing clean, efficient, and well-documented code
  • Performing code review and validation tasks
  • Collaborating with project teams and communicating progress updates
  • Staying updated with new statistical programming techniques
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Eligibility Criteria

Education

  • Bachelor’s degree in a scientific discipline (Statistics, Life Sciences, Mathematics, or related field preferred)

Experience

  • Entry-level or early-career candidates can apply
  • Basic understanding of clinical research and statistical programming preferred

Skills Required

  • Strong knowledge of SAS programming (Base SAS, Macros)
  • Familiarity with R, Python, or other statistical tools (preferred)
  • Understanding of GCP, FDA, EMA, and ICH guidelines
  • Analytical thinking and data interpretation skills
  • Good communication and teamwork abilities
  • Attention to detail and problem-solving capability

Salary & Benefits

  • Salary: Not disclosed
  • Opportunity to work on global clinical research projects
  • Exposure to regulatory submissions and CDISC standards
  • Career growth in biostatistics and clinical programming
  • Collaborative and innovation-driven work environment

Selection Process

The hiring process generally includes:

  1. Online Application
  2. Resume Screening
  3. Technical Interview (Programming & Statistics)
  4. HR Discussion
  5. Final Selection

Candidates may be evaluated on SAS programming skills and clinical data understanding.


How to Apply

Interested candidates can apply through the official career portal of the company. Ensure your resume highlights your programming skills, academic background, and any relevant projects.


Important Dates

  • Job ID: 2893
  • Last Date to Apply: Not specified

Why Apply for This Pharma Job?

This role is an excellent entry point into the high-demand field of clinical data science and biostatistics. It provides hands-on experience in statistical programming, regulatory submissions, and clinical trial data analysis.

Professionals in this field can build long-term careers in clinical research, data science, and regulatory analytics. With increasing demand for data-driven healthcare solutions, this role offers strong growth potential.


Important Note / Disclaimer

IndiaPharmaJobs.in is an independent job information platform and is not affiliated with any company or recruiter. We do not charge any fee for job applications. Candidates should verify all details independently before applying.

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Final Call-to-Action

If you have an interest in clinical data, SAS programming, and biostatistics, this is a great opportunity to start or grow your career. Apply now and take your first step into clinical research and data science.


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