Sr SAS Programmer - Chennai *
About the role
This vacancy has now expired. Please click here to view live vacancies.
- Recognize, exemplify and adhere to ICON's values which centersaround our commitment to People, Clients and Performance.
- As a member of staff, the employee is expected to embrace and contribute to our culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs.
- As an experienced staff member, the employee is expected to recognize the importance of and create a culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs.
- Travel (approximately 0%) domestic and/or international
- Works effectively on multiple projects delivering quality output in a timely fashion
- Programs analysis datasets, listings and tables without supervision and offers advice to others within team
- Able to work on complex programming assignments and share knowledge appropriately
- Plans ahead, performs early review of all assigned project work - escalates any issues
- Is responsible to ensure that all output with a project is accurate and has consistent appearance
- Creates and maintains study documentation and files according to departmental policy
- Maintains professional currency through literature reviews and membership to professional bodies
- Identifies training needs within SAS team and puts in place specific initiatives to helps Indian staff to develop their skills
- Attends project team meetings, as required, and looks for opportunities to improve programming process across projects.
- Uses technical skills to bring forward better methodologies and approaches to coding. Leads process and programming improvement through broader knowledge.
- Other duties as assigned
- Works as a mentor for programmers across the organization
- To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
- Educational Requirements
- Bachelor's degree, in a quantitative or scientific discipline, or local equivalent
- Substantial experience in SAS Programming, or equivalent, preferably in the Clinical Domain.
- Proven ability to produce report quality tables graphs and data listings without direct supervision
- Proven ability to drive process improvements within area of expertise
- Understanding of data structures within the Clinical Domain as well as a solid understanding of the development and use of standard programs
- Advanced problem solving skills, attention to detail, good verbal and written
- Excellent communications skills
- Ability to transfer own knowledge to others and help them improve
- Advanced SAS certification
Explore more about ICON
Day in the life
Teaser label
IndustryContent type
BlogsPublish date
07/22/2026
Summary
Clinical Trials: From Protocol to Patient Clinical trials are essential to the development of new medicines and treatments, yet the way they work is often misunderstood. For those considering a ca
Teaser label
IndustryContent type
BlogsPublish date
07/21/2026
Summary
A Beginner's Guide to Drug Safety When most people think about careers in clinical research, roles like Clinical Research Associate or Clinical Trial Manager usually come to mind. But there's ano
Teaser label
Our PeopleContent type
BlogsPublish date
07/06/2026
Summary
Meet the CRA helping shape a new partnership Ask Rebeca Rojas Hernández what her dad tells people she does for a living and she can't help but smile. "He proudly tells everyone that I visit clinic
Similar jobs at ICON
Salary
Location
US, Blue Bell (ICON)
Department
Full Service - Development & Commercialisation Solutions
Location
Blue Bell
Remote Working
Remote or Office
Business Area
ICON Full Service & Corporate Support
Job Categories
Medical Imaging
Job Type
Permanent
Description
As an Imaging Scientist II at ICON, you will lead the design, execution, and analysis of clinical trials involving medical imaging modalities, contributing to the advancement of innovative treatments
Reference
JR150874
Expiry date
01/01/0001
Author
Kris CostelloAuthor
Kris CostelloSalary
Location
US, Blue Bell (ICON)
Location
Blue Bell
Miami, FL
Remote Working
Remote
Business Area
ICON Strategic Solutions (FSP)
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a CRA II at ICON, you will design and analyze clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. This position is sponsor
Reference
JR156224
Expiry date
01/01/0001
Author
Jamie PruittAuthor
Jamie PruittSalary
Location
Philadelphia, PA
Location
Boston, MA
Philadelphia, PA
Warren
Remote Working
Remote
Business Area
ICON Strategic Solutions (FSP)
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.What You Will Be
Reference
JR156105
Expiry date
01/01/0001
Author
Jonathan HolmesAuthor
Jonathan HolmesSalary
Location
Regional United States (PRA)
Location
Multiple US Locations
Remote Working
Remote
Business Area
ICON Strategic Solutions (FSP)
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
We are currently seeking a Lead Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Lead CRA at ICON, you will play a pivotal role in overseeing and managing clinical trial si
Reference
JR156029
Expiry date
01/01/0001
Author
Jonathan HolmesAuthor
Jonathan HolmesSalary
Location
Canada, Burlington
Location
Burlington
Remote Working
Remote
Business Area
ICON Strategic Solutions (FSP)
Job Categories
Clinical Project Management
Job Type
Permanent
Description
We are currently seeking a Project Manager to join our diverse and dynamic team. As a Project Manager at ICON, you will be responsible for leading and coordinating project activities, ensuring that pr
Reference
JR155771
Expiry date
01/01/0001
Author
Kaitlyn LurkerAuthor
Kaitlyn LurkerSalary
Location
Canada, Burlington
Location
Burlington
Remote Working
Remote
Business Area
ICON Strategic Solutions (FSP)
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
What you will be doing Support Global Study Director (GSD) / Global Study Associate Director (GSAD) and Global Study Managers (GSMs) by completing delegated study work.Initiate and lead the set-up of
Reference
JR156253
Expiry date
01/01/0001
Author
Jonathan HolmesAuthor
Jonathan Holmes