Location: Bangalore, India
Company: Fortrea
Job Type: Full-Time
Experience Required: Minimum 5 Years
Eligibility: Experienced Professionals Only (Freshers Not Eligible)
Application Deadline: May 31, 2026
About the Company
Fortrea is a leading global Contract Research Organization (CRO) providing clinical development, patient access, and technology solutions to pharmaceutical, biotechnology, and medical device companies worldwide. The organization is known for delivering innovative clinical trial solutions and advanced statistical programming services across global studies.
Job Overview – Programming Lead
Fortrea is hiring experienced Statistical Programming professionals for the role of Programming Lead in Bangalore. This position is ideal for candidates with strong expertise in SAS programming, CDISC standards, SDTM, ADaM datasets, and clinical trial data analysis within the CRO or pharmaceutical industry.
The selected candidate will lead end-to-end programming activities for clinical studies while ensuring high-quality deliverables, regulatory compliance, and timely project execution.
Key Responsibilities
Perform the role of Lead Statistical Programmer for global clinical studies
Plan, execute, and oversee programming activities across assigned projects
Manage timelines, budgets, quality standards, and resource allocation
Develop and maintain SAS programs for:
SDTM datasets
ADaM datasets
Tables, Listings, and Figures (TFLs)
Conduct quality control (QC) reviews of SDTM, ADaM, and TFL outputs
Create and maintain:
Define.xml files
Define PDFs
Analysis Results Metadata (ARM)
Annotated CRFs
Reviewer Guides
Develop programming specifications for SDTM and ADaM datasets
Review Statistical Analysis Plans (SAPs) and TFL shells from a programming perspective
Mentor junior and less-experienced statistical programmers
Participate in department knowledge-sharing sessions and technical presentations
Support QA audits, client audits, and regulatory inspection readiness
Identify process improvement opportunities to enhance productivity and efficiency
Required Qualifications
Bachelor’s degree in:
Mathematics
Statistics
Computer Science
Life Sciences
Health Sciences
Related disciplines
Equivalent education and industry experience may also be considered
Required Skills
Strong expertise in SAS Programming
Advanced knowledge of:
CDISC standards
SDTM
ADaM
TFL development
Understanding of clinical trial data workflows and regulatory requirements
Strong analytical, communication, and leadership skills
Experience working in CRO or pharmaceutical environments
Experience Required
Minimum 5 years of SAS Statistical Programming experience in the CRO, biotechnology, or pharmaceutical industry
Candidates with leadership experience in clinical programming projects will be preferred
Freshers are not eligible for this role
Work Environment & Travel
Office-based or home-based work model depending on business requirements
Approximately 5% travel may be required for:
Client meetings
Trainings
Internal collaboration activities
Some travel may involve overnight stays depending on project requirements
Why Apply for This Role?
Opportunity to work on global clinical trials and regulatory submissions
Exposure to advanced statistical programming and CDISC implementation
Leadership role with mentoring responsibilities
Career growth opportunities in a globally recognized CRO
Collaborative and innovation-driven work culture
How to Apply
Interested candidates can apply directly through the official careers portal of Fortrea.
For more verified global Clinical Research, Biostatistics, SAS Programming, Pharmacovigilance, Medical Writing, Regulatory Affairs, and Pharma IT jobs, visit ThePharmaDaily.com.
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