Sr SAS Programmer - Chennai *
About the role
This vacancy has now expired. Please see similar roles below...
- 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
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
Teaser label
IndustryContent type
BlogsPublish date
11/19/2024
Summary
Decoding Clinical Research Abbreviations: Essential Terms Explained Clinical research professionals use hundreds of abbreviations every day. Simple letters like AE mean Adverse Event, while longer
Teaser label
Our PeopleContent type
BlogsPublish date
11/13/2024
Summary
How to Become a Clinical Research Associate: A Step-by-Step Guide The clinical research industry is projected to reach $52.0 billion by 2026, growing at an impressive rate of 5.6% annually. This
Teaser label
Career ProgressionContent type
BlogsPublish date
11/12/2024
Summary
Building a Career in Clinical Data Management Clinical data management roles and responsibilities have become increasingly crucial in modern healthcare research and development. The healthcare ind
Similar jobs at ICON
Salary
Location
United States
Department
Clinical Trial Management
Location
United States
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
As a Sr CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Reference
2024-115319
Expiry date
01/01/0001
Author
Monica HawkinsAuthor
Monica HawkinsSalary
Location
Regional United States (PRA)
Department
Clinical Monitoring
Real World Solutions
Location
Multiple US Locations
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
We are currently seeking a Clinical Research Associate to join our diverse and dynamic Biotech team that is therapeutically aligned in our Gen Med space. As a Clinical Research Associate , you’ll work
Reference
JR122124
Expiry date
01/01/0001
Author
Tina GeerAuthor
Tina GeerSalary
Location
US, Blue Bell (ICON)
Location
Multiple US Locations
Blue Bell
Remote Working
Hybrid: Office/Remote
Business Area
ICON Full Service & Corporate Support
Job Categories
Drug Safety
Job Type
Permanent
Description
The MI staff member will work in a Medical Call Center and is responsible for all medical information duties to support clients in compliance with applicable regulation, the company Standard Operation
Reference
JR126053
Expiry date
01/01/0001
Author
Mitzi OvertonAuthor
Mitzi OvertonSalary
Location
United States
Department
Clinical Trial Management
Location
United States
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
As a Local Trial Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Reference
2024-115310
Expiry date
01/01/0001
Author
Monica HawkinsAuthor
Monica HawkinsSalary
Location
Brazil
Department
Clinical Monitoring
Location
Brazil
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
A Clinical Research Associate is a professional who contributes to accelerated drug/device/outcomes research through independent monitoring of studies to ensure patient safety and data integrity. You
Reference
2024-115351
Expiry date
01/01/0001
Author
Bruna DuarteAuthor
Bruna DuarteSalary
Location
Brazil
Department
Clinical Monitoring
Location
Brazil
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
A Clinical Research Associate is a professional who contributes to accelerated drug/device/outcomes research through independent monitoring of studies to ensure patient safety and data integrity. You
Reference
2024-115349
Expiry date
01/01/0001
Author
Bruna DuarteAuthor
Bruna Duarte