JUMP TO CONTENT
Shortlist
search jobs Search

Our Culture Application Process Career Resources Our Mission & Values

Sr SAS Programmer - Chennai *

011824_2

About the role

This vacancy has now expired. Please click here to view live vacancies.
This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. As a Sr. SAS Programmer you will assist US or EU statistical programming team by developing SAS programs for analysis datasets, listings and safety summary tables; provides project tracking information to the team, address any validation comments and documents programming activities; works on more advanced, complex SAS requirements, across multiple studies, and acts as a subject matter expert within the Indian SAS programming team; mentors and helps train other team members from juniors to SAS Programmer II.
 
Overview of the role
  • 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
Supervision
  • Works as a mentor for programmers across the organization  
Role Requirements
  • 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
Benefits of Working in ICON
 
Other than working with a great team of smart and energetic people, we also offer a very competitive salary and benefits package that includes an excellent pension scheme, private health care, life assurance and staff recognition schemes.  This varies from country to country so a dedicated recruiter will discuss this with you at interview stage.
 
We care about our people as they are the key to our success. We provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long term career.   
 
What’s Next
 
Following your application you will be contacted by one of our dedicated recruiters and if successful we will be able to provide you with more details about this opportunity.
 
ICON is an equal opportunity employer -  M/F/D/V and committed to providing a workplace free of any discrimination or harassment.
*LI-GA1
List #1

Day in the life

Headshot image of male
Driving Trials Forward: Study Start-Up Leadership at ICON

Teaser label

Our People

Content type

Blogs

Publish date

03/16/2026

Summary

Driving Study Start-Up: James Pereira's Journey at ICON James Pereira's career in clinical research has been shaped by a single driving question: how do we get studies started faster? From his earl

Teaser label

Explore James Pereira's career in study start-up at ICON, leading global teams to accelerate patient access.

Read more
Male and female in lab
Who’s Who in a Clinical Trial Team

Teaser label

Inside ICON

Content type

Blogs

Publish date

03/15/2026

Summary

Who's Who In a Clinical Trial Team Clinical trials rely on large, cross functional teams working together across countries, time zones and specialisms. For those new to the industry, the number of

Teaser label

Understand the key roles in a clinical trial team, from study start up and site activation to data, safety and quality.

Read more
Nurse and patient
Understanding Roles in a Clinical Trial: Sponsors, CROs, and Sites

Teaser label

Industry

Content type

Blogs

Publish date

02/16/2026

Summary

What Sponsors, CROs, and Sites Each Do Clinical research brings together many organisations, each with a specific role in delivering a clinical trial. For those new to the industry, the relationsh

Teaser label

Learn how clinical trials are delivered by understanding the roles of sponsors, CROs, and sites.

Read more
View all

Similar jobs at ICON

Senior Research Scientist

Salary

Location

US, Lenexa KCIB (PRA)

Department

Full Service - Early Clinical and Bioanalytical Solutions

Location

Lenexa

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Research and Development

Job Type

Permanent

Description

At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own I

Reference

JR139131

Expiry date

01/01/0001

Hanna Pitcairn

Author

Hanna Pitcairn
Hanna Pitcairn

Author

Hanna Pitcairn
Read more Shortlist Save this role
Read more Shortlist Save this role
Clinical Scientist I

Salary

Location

Brazil, Sao Paulo

Location

Sao Paulo

Remote Working

Remote or Office

Business Area

ICON Strategic Solutions

Job Categories

Scientist

Job Type

Permanent

Description

We are currently seeking a Clinical Scientist to join our diverse and dynamic team. As a Clinical Scientist at ICON, you will play a critical role in designing and conducting clinical studies that adv

Reference

JR147279

Expiry date

01/01/0001

Bruna Duarte

Author

Bruna Duarte
Bruna Duarte

Author

Bruna Duarte
Read more Shortlist Save this role
Read more Shortlist Save this role
Project Manager, Laboratory

Salary

Location

Mexico, Mexico City

Department

Full Service - Development & Commercialisation Solutions

Location

Mexico City

Remote Working

Hybrid

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Project Management

Project Management

Job Type

Permanent

Description

Project Manager, Laboratory Location: Mexico City - Benito Juarez(Hybrid model 3 days peer week working at office - 2 days from home) This is an exciting opportunity to work within a fast paced, busy

Reference

JR133822

Expiry date

01/01/0001

Daniela Guerrero

Author

Daniela Guerrero
Daniela Guerrero

Author

Daniela Guerrero
Read more Shortlist Save this role
Read more Shortlist Save this role
Clinical Trial Associate (Study Start-Up Support)

Salary

Location

US, Blue Bell (ICON)

Location

Raleigh

Blue Bell

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Study Start Up

Job Type

Permanent

Description

What you will be doing The SSU Clinical Study Administrator is responsible for ensuring vendor spreadsheets are completed correctly and processed (submitted to vendor or global team) according to stud

Reference

JR147161

Expiry date

01/01/0001

Jonathan Holmes

Author

Jonathan Holmes
Jonathan Holmes

Author

Jonathan Holmes
Read more Shortlist Save this role
Read more Shortlist Save this role
Financial Analyst II

Salary

Location

Ireland, Dublin

Location

Dublin

Remote Working

Hybrid

Business Area

ICON Full Service & Corporate Support

Job Categories

Accounting & Finance

Job Type

Permanent

Description

The Role:The successful candidate will provide financial analysis to Operational & Finance management on the historical and current financial performance and future outlook of portfolios of work withi

Reference

JR147239

Expiry date

01/01/0001

Damien Kehir

Author

Damien Kehir
Damien Kehir

Author

Damien Kehir
Read more Shortlist Save this role
Read more Shortlist Save this role
Senior CRA

Salary

Location

Mexico, Mexico City

Department

Clinical Monitoring

Location

Mexico City

Remote Working

Remote or Office

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical

Reference

JR144174

Expiry date

01/01/0001

Diego Tonini

Author

Diego Tonini
Diego Tonini

Author

Diego Tonini
Read more Shortlist Save this role
Read more Shortlist Save this role
View Jobs

Browse popular job categories below or search all jobs above