Statistical Programmer 1 (DM SAS Listings Team)

FTINDDDBLR Fortrea Development India Private Limited_BLR

Bengaluru

On-site

INR 700,000 - 1,200,000

Full time

10 days ago

Get more replies from employers

Send a job-specific resume in minutes.

Benefits offered by this job

Hybrid work arrangement

Job summary

Fortrea Development India Private Limited_BLR in Bengaluru is seeking a SAS Programmer to provide statistical programming support for clinical trial projects. You will develop, validate, and maintain SAS programs and outputs for management, analysis, and reporting of clinical trial data.

You will develop and maintain data transfer programs, DM SAS listings, and review outputs to ensure quality and accuracy.

Qualifications

  • Bachelor's degree in CS, Life Sciences, Math, Statistics or related field.
  • 1–3 years of SAS programming experience in CRO/pharma environment.
  • Experience in developing and maintaining vendor data programs.
  • Proficiency in English (speaking, writing, reading).

Responsibilities

  • Provide Statistical Programming support for clinical trial projects.
  • Develop, validate, and maintain SAS programs and outputs for management, analysis, and reporting of clinical trial data.
  • Develop and maintain data transfer programs in accordance with client specifications and project requirements.
  • Develop DM SAS listings as per client specifications and study standards.
  • Review draft and final production outputs to ensure quality, accuracy, and consistency.
  • Take ownership of the quality and integrity of all assigned deliverables.
  • Collaborate with cross-functional teams including Clinical Data Management and Statistical Programming.
  • Prioritize and manage multiple studies and tasks in a fast-paced environment to meet timelines and deliverables.
  • Demonstrate a positive and professional attitude and contribute to a collaborative team environment.
  • Continuously develop technical, industry, and project-related knowledge and skills.
  • Maintain high attention to detail and ensure work meets high quality standards.
  • Develop problem-solving skills and seek guidance from senior Statistical Programming staff when required.
  • Gain knowledge of broader Statistical Programming activities under guidance of senior team members.
  • Adhere to Fortrea SOPs, GCP, and QMS requirements.
  • Support process improvement initiatives and contribute to operational excellence.
  • Perform additional duties as assigned by senior staff or management.

Skills

SAS programming
Data analysis
Cross-functional collaboration
Attention to quality

Education

Bachelor's degree in Computer Science, Life Sciences, Mathematics, Statistics or related field

Tools

SAS
SAS Macro Development

Job description

Summary of Responsibilities
  • Provide Statistical Programming support for clinical trial projects.
  • Develop, validate, and maintain SAS programs and outputs for the management, analysis, and reporting of clinical trial data.
  • Develop and maintain data transfer programs in accordance with client specifications and project requirements.
  • Develop Data Management (DM) SAS listings as per client specifications and study standards.
  • Review draft and final production outputs to ensure quality, accuracy, and consistency.
  • Take ownership of the quality and integrity of all assigned deliverables.
  • Collaborate effectively with cross-functional teams, including Clinical Data Management, Statistical Programming, and other project stakeholders.
  • Effectively prioritize and manage multiple studies, tasks, and competing priorities in a fast-paced environment, consistently delivering high-quality results while meeting project timelines and deliverables.
  • Demonstrate a positive and professional attitude, contributing to a collaborative and productive team environment.
  • Continuously develop technical, industry, and project-related knowledge and skills.
  • Maintain a high level of attention to detail and ensure all work is delivered to the highest quality standards.
  • Develop strong problem-solving skills and proactively seek guidance from senior Statistical Programming staff when required.
  • Gain knowledge of broader Statistical Programming activities and responsibilities under the guidance of senior team members.
  • Adhere to Fortrea Standard Operating Procedures (SOPs), Good Clinical Practice (GCP), and Quality Management System (QMS) requirements.
  • Support process improvement initiatives and contribute to operational excellence within the department.
  • Perform additional duties and responsibilities as assigned by senior Statistical Programming staff or management.
Qualifications (Minimum Required)
  • Bachelor's degree in computer science, Life Sciences, Mathematics, Statistics, or a related discipline.
  • Fortrea may consider relevant and equivalent experience in lieu of educational requirements.
Language Skills Required

Speaking: English required Writing/Reading: English required

Experience (Minimum Required)
  • 1 to 3 years of SAS programming experience in the CRO or Pharmaceutical Industry, or an equivalent combination of education, with a solid understanding of programming fundamentals and program development principles.
  • Mandatory experience in developing and maintaining vendor data programs.
  • Experience in coding, database reconciliation, PK deviation analysis, and development of custom listings is advantageous.
  • Experience in SAS macro development, debugging, and working with complex macros would be an advantage.
  • SAS certification is desirable but not mandatory.
  • Understanding of the clinical trial process.
  • Ability to work effectively with cross-functional teams and stakeholders.
  • Results-driven with a strong focus on delivery and accountability.
  • Strong attention to quality and continuous improvement.
Physical Demands/Work Environment

Office environment (Hybrid) Learn more about our EEO & Accommodations request here.

At Fortrea, we're all about turning the “impossible” into "I'm possible." Together, we break barriers to deliver exceptional service to our patients, fueled by a shared commitment to teamwork and excellence. Regardless of your role, we're all family, working together to achieve extraordinary results. At Fortrea, your career isn't just a job – it's a journey of making the exceptional possible, every day.

Get your free, confidential resume review.
or drag and drop your file here.
Similar jobs

Similar jobs worth comparing

Statistical Programmer 1 (DM SAS Listings Team)
Statistical Programmer 1 (DM SAS Listings Team)

Fortrea Development India • Bengaluru

Hybrid
INR 600,000 - 900,000
Statistical Programmer 1 DM SAS Listings Team
Statistical Programmer 1 DM SAS Listings Team

Fortrea • Bengaluru

Hybrid
INR 600,000 - 1,200,000
Hybrid work environment
Principal Statistical Programmer FSP
Principal Statistical Programmer FSP

Cytel • Mumbai City

On-site
INR 2,500,000 - 4,500,000
Statistical Programmer II
Statistical Programmer II

eClinical Solutions • Bengaluru

On-site
INR 1,400,000 - 2,100,000
Programmer Analyst l (RAVE/Veeva)
Programmer Analyst l (RAVE/Veeva)

Fortrea • Mumbai

On-site
INR 700,000 - 1,000,000
Statistical Programmer- Future Roles (India)
Statistical Programmer- Future Roles (India)

Syneos Health, Inc. • Gurugram District

On-site
INR 600,000 - 900,000
Principal Statistical Programmer FSP
Principal Statistical Programmer FSP

Cytel • India

On-site
INR 1,200,000 - 1,500,000
Principal Statistical Programmer
Principal Statistical Programmer

SDC (Statistics & Data Corporation) • Hyderabad

On-site
INR 600,000 - 1,000,000
Flexible Work Schedule
Career Advancement Opportunities
Employee Recognition Program
+2
SAS Programmer
SAS Programmer

Sciens Software Technologies • Hyderabad

Hybrid
INR 900,000 - 1,300,000
Principal Statistical Programmer
Principal Statistical Programmer

Cytel • India

On-site
INR 900,000 - 1,500,000