Sr. SAS Programmer ll Home Based
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. Our Senior SAS Programmer Analysts play a key role within ICON developing and executing execute statistical programs designed to analyze clinical trial information.
The Senior SAS Programmer will be responsible for designing and developing standard software and data structures, developing and executing statistical programs designed to analyze clinical trial information and participating in the development and maintenance of SOPs (including software validation, documentation, study archiving and others as needed). This position can be located at the ICON facility in Warrington, PA or Raleigh, NC or be home based anywhere in the US
Overview of the role
- Develop and execute statistical analyses of clinical trial data. Design and develop computer programs that produce tables, figures, listings and derived datasets that summarize results of clinical trials.
- Participate in the review of Case Report Forms (design phase), Statistical Analysis Plans, QC Specifications and Database Structures.
- Assess data from clinical trials for consistency and accuracy.
- Develop and implement quality assurance software.
- Design and implement analysis file structures.
- Monitor procedures for software validation.
- Work on cross-disciplinary teams to assure programming needs are met and appropriate requests are made.
Role Requirements
- Bachelor’s of Science degree in a quantitative discipline (or training equivalent to) or equivalent work experience.
- 5+ years full time SAS programming experience for Senior Programmer; experience must be in the pharmaceutical or biotechnology industry.
- Understanding of data structures, standard software and their implementation.
- Knowledge of the drug development process (Phase I through IV) and general regulatory requirements.
- Good written and verbal communications skills
Impactful work. Meaningful careers. Quality rewards.
At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential. See all locations Learn more about Our Culture at ICON
Day in the life
.png)
Teaser label
IndustryContent type
BlogsPublish date
04/22/2025
Summary
What is an IND or NDA? A Guide for Aspiring Clinical Research Professionals If you’re considering a career in clinical research or the broader pharmaceutical and biotech industry, you’ve likely c
.png)
Teaser label
IndustryContent type
BlogsPublish date
04/22/2025
Summary
When it comes to clinical trials, one of the most important documents you’ll hear about is the Informed Consent Form (ICF). Whether you're starting out in clinical research or exploring job opportunit
.png)
Teaser label
IndustryContent type
BlogsPublish date
04/17/2025
Summary
CRA vs CRC Embarking on a career in clinical research is an exciting journey for STEM graduates, offering opportunities to contribute directly to the development of new therapies and to safeguard
Similar jobs at ICON
Salary
Location
Chile
Department
Clinical Trial Management
Location
Chile
Remote Working
Office Based
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
As a Clinical Trial Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. You will be part of an innovative and globa
Reference
2025-118938
Expiry date
01/01/0001
Author
Magda ObregonAuthor
Magda ObregonSalary
Location
Puerto Rico
Department
Project Management Roles
Location
Puerto Rico
Remote Working
Office Based
Business Area
ICON Strategic Solutions
Job Categories
Project Management
Job Type
Permanent
Description
As a Project Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. You will be partnering with one of our global phar
Reference
2025-118937
Expiry date
01/01/0001
Author
Magda ObregonAuthor
Magda ObregonSalary
Location
Mexico
Department
Biometrics Roles
Location
Mexico
Remote Working
Remote
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 Senior Clinical Data Coordinator (Sr CDC) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Working within one of ou
Reference
2025-118936
Expiry date
01/01/0001
Author
Magda ObregonAuthor
Magda ObregonSalary
Location
United States
Department
Regulatory, Drug Safety/ Quality Assurance & Other roles
Location
United States
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Other
Job Type
Permanent
Description
As a Sr. TAT Expert you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Reference
2025-118429
Expiry date
01/01/0001
Author
Melissa BennerAuthor
Melissa BennerSalary
Location
Bogota
Department
Clinical Trial Management
Location
Bogota
Remote Working
Office Based
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
As a Clinical Trial Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. You will be partnering with one of our glo
Reference
2025-118470
Expiry date
01/01/0001
Author
Magda ObregonAuthor
Magda ObregonSalary
Location
Mexico, Mexico City
Location
Mexico City
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Trial Support
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
JR129630
Expiry date
01/01/0001
Author
Ana LuciaAuthor
Ana Lucia