JUMP TO CONTENT

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

People talking in a meeting
Networking Strategies in Clinical Research

Teaser label

Industry

Content type

Blogs

Publish date

06/06/2025

Summary

Building Connections that Drive Progress In an industry where collaboration is critical to advancing science and improving patient outcomes, networking is more than a professional courtesy - it’s

Teaser label

Discover how strategic networking can strengthen collaboration, and support your clinical research career journey.

Read more
Blood cancer cells
Blood Cancer Day - Raising Awareness and Driving Change

Teaser label

Industry

Content type

Blogs

Publish date

05/29/2025

Summary

Blood Cancer Day Blood Cancer Day is a powerful reminder of the millions of individuals and families whose lives are affected by hematological malignancies every year. These diseases are complex,

Teaser label

Learn how clinical research is transforming the future for those affected by hematological cancers.

Read more
Silver ribbon
Recognising World Schizophrenia Day through Research and Compassion

Teaser label

Industry

Content type

Blogs

Publish date

05/22/2025

Summary

World Schizophrenia Awareness Day 2025 Every year on 24 May, World Schizophrenia Awareness Day offers a vital opportunity to raise awareness, dismantle stigma, and celebrate the strength of individ

Teaser label

Explore how ICON is advancing schizophrenia research and addressing stigma through clinical innovation.

Read more
View all

Similar jobs at ICON

Clinical Data Manager- Ecoa

Salary

Location

United States

Department

Biometrics Roles

Location

United States

Remote Working

Home-Based

Business Area

ICON Strategic Solutions

Job Categories

Clinical Data Management

Clinical Data Scientist Lead

Clinical Systems

Data Standards Consultant

Job Type

Permanent

Description

As a Clinical Data Science Lead you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

Reference

2025-120018

Expiry date

01/01/0001

Brendan Hoey

Author

Brendan Hoey
Read more Shortlist Save this role
Contract Analyst II

Salary

Location

Mexico City

Department

Clinical Operations Roles

Location

Mexico City

Remote Working

Home-Based

Business Area

ICON Strategic Solutions

Job Categories

Contracts Administration

Job Type

Permanent

Description

As a Senior Contracts Analyst in Mexico you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. In this role you will be respon

Reference

2025-120356

Expiry date

01/01/0001

Rita Villavicencio Read more Shortlist Save this role
Medical Technologist I

Salary

Location

US, San Antonio, TX, IDS

Department

Full Service - Early Clinical and Bioanalytical Solutions

Location

San Antonio

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Laboratory

Job Type

Permanent

Description

Are you interested in assisting in the day-to-day activities of the analytical laboratory including responsibility for performing assays on samples for pharmaceutical and chemical companies?ICON has a

Reference

JR129931

Expiry date

01/01/0001

Hanna Pitcairn Read more Shortlist Save this role
Medical Admin Assistant I

Salary

Location

Mexico, Mexico City

Department

Drug Safety & Pharmacovigilence

Location

Mexico City

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Pharmacovigilance & Patient Safety

Job Type

Permanent

Description

What You Will Be Doing:Assist in organizing and coordinating medical team meetings and activities.Manage and maintain medical documentation and records.Coordinate communication and information flow be

Reference

JR130842

Expiry date

01/01/0001

Daniela Guerrero Read more Shortlist Save this role
Senior Site Contracts Negotiator

Salary

Location

Turkey, Ankara

Location

Ankara

Remote Working

Home or Office

Business Area

ICON Full Service & Corporate Support

Job Categories

Contracts Administration

Job Type

Permanent

Description

Role Summary:Responsible for the successful negotiation and on-going maintenance of clinical trial agreements, complex amendments, and other ancillary agreements with investigative sites.Responsibilit

Reference

JR129118

Expiry date

01/01/0001

Magda Kozuszek Read more Shortlist Save this role
Clinical Trial Call Center Representative - Entry Level

Salary

Location

US, Salt Lake City (PRA)

Department

Full Service - Early Clinical and Bioanalytical Solutions

Location

Salt Lake City

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Study Start Up

Job Type

Permanent

Description

We are currently seeking a Clinical Trial Recruitment Representative to join our diverse and dynamic team at ICON at our Salt Lake City UT site. Location: On-Site Salt Lake City UTJob Type: Full Time

Reference

JR131004

Expiry date

01/01/0001

Kris Costello

Author

Kris Costello
Read more Shortlist Save this role
View Jobs

Browse popular job categories below or search all jobs above