Principal Statistical Programmer

Emmes; Bengaluru; On-site; INR 1,000,000 - 1,500,000; Full time

Job summary

Emmes is seeking a Principal Statistical Programmer I in Bengaluru, India, to provide lead statistical programming support for clinical research projects. The successful candidate will utilize advanced SAS programming techniques and mentor staff while ensuring regulatory-compliant output and methodologies are adopted.

Applicants should have a strong analytical background, excellent communication skills, and at least 6 years of experience in statistical programming within a Pharmaceutical or CRO environment.

Qualifications

• 6+ years of statistical programming experience in a Pharmaceutical/CRO environment.
• Strong knowledge of CDISC standards and clinical trial methodologies.
• Good understanding of GCP principles.

Responsibilities

• Lead statistical programming support for complex clinical research studies.
• Develop and write programming documentation and efficient code.
• Present statistical programming topics internally and externally.

Skills

Statistical programming in SAS

Analytical skills

Communication

Problem-solving

Education

Bachelor's or Master's/Doctoral degree in a scientific discipline

Tools

SAS (Base, Macros, SQL)

R

Python

Job description

Overview

Emmes Group: Building a better future for us all. Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into public‑private partnerships and commercial biopharma. Emmes has built industry leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience. We believe the work we do will have a direct impact on patients’ lives and act accordingly. We strive to build a collaborative culture at the intersection of being a performance and people‑driven company. We’re looking for talented professionals eager to help advance clinical research as we work to embed innovation into the fabric of our company. If you share our motivations and passion in research, come join us!

Primary Purpose

The Principal Statistical Programmer I provides lead statistical programming support for complex clinical research projects, utilizes advanced SAS programming techniques and offers expert consultation across the company. Key responsibilities include ensuring the use of sound methodologies, delivering key regulatory‑compliant output, developing organized programming documentation, writing efficient code, and mentoring staff. This role also provides project updates to management while performing assigned duties and presents internally on statistical programming topics. Expertise in statistical programming techniques and strong communication skills are essential for success in this role.

Responsibilities

• Provides lead statistical programming support for multiple complex clinical research studies or study teams.
• Provides advanced statistical programming development with SAS (Base, Macros and SQL) and provides expert consultation to projects across the company including statistical programming methodology.
• Ensures that sound methodologies are adopted by establishing advanced knowledge of programming techniques required for clinical trials research which involve CDISC standards and analysis data sets or production of standard and custom tables, listings and figures.
• Provides key deliverables based on established advanced knowledge of regulatory requirements for clinical research E‑submissions and/or study requirements for Sponsor, Regulatory, Investigator or Safety review meetings.
• Develops well organized programming documentation and annotations including specifications, review of mock shells, adhering to relevant Standard Operating Procedures and contributes to standardization efforts.
• Writes well‑documented, efficient, and high‑quality code, conducts code review, supports cross‑functional programming activities, and programming validation as needed.
• Develops expertise in current statistical programming techniques to develop reproducible code and ensure the adoption of sound methodologies.
• Presents statistical programming topics internally and may present at external conferences.
• Serves as a mentor to statistical programming staff.
• Provides project updates to appropriate project management or department management staff.
• Other duties as assigned.

Qualifications

• A bachelor's degree plus 6 years or master's/doctoral degree plus 4 years Statistical programming experience as a CDISC/TLF Statistical programmer in Pharmaceutical/CRO environment, education in a scientific discipline preferred.
• Understanding of GCP principles and other regulatory standards (e.g. FDA, EMA, and ICH guidance and recommendations) in Clinical Research.
• Good analytical skills with the ability to process scientific and medical data.
• Ability to manage multiple tasks and priorities independently.
• Ability to work independently as well as in a team environment.
• Strong skills in prioritization, problem‑solving, organization, decision‑making, and time management.
• Ability to articulate complex and advanced programming and technical concepts through written and oral communication.
• Excellent communication, interpersonal and organization skills.
• Self‑motivated, proactive and detail oriented.
• Strong statistical programming skills in SAS, familiarity with R, Python or other relevant statistical software considered beneficial.

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