SAS Programmer II
- Any EMEA Location, South Africa
- Programming
- ICON Strategic Solutions
TA Business Partner
- Icon Strategic Solutions
About the role
This vacancy has now expired. Please click here to view live vacancies.
ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.
- Services rendered will adhere to applicable SOPs, WIs, policies, local regulatory requirements,
- Provides expertise in planning, creation and oversight of clinical programming activities and deliverables from study set-up to submission ready CDISC SDTM tabulation packages (aCRF, define.xml, cSDRG, etc.).
- Review and provide input into all trial set-up documentation.
- Responsible for review or creation of aCRF, DTA metadata and trial design specifications.
- Create or review mapping specifications for internal data and/or SDTM
- Generate or review internal data and/or SDTM datasets using internal conversion framework, utilities, and global checks Ensure quality review of all datasets (e.g., Pinnacle 21 compliance checking); ensure datasets are available for stakeholder use (medical review, central monitoring, adaptive design, etc.) and compliant for interim and final database
- Program, or oversee programming of, quality review checks and reports for use by Data Managers and other team
- Responsible for creation of submission-ready SDTM packages for FDA/PMDA or other regulatory authority submissions and keeping abreast in changing regulatory
- Responsible for acquiring and maintaining working knowledge in the various and future evolving data collection tools applied in the clinical trial space such as Medidata Rave, Clinical Data Tools such as LSAF, Pinnacle 21, and in CDISC standards such as SDTM, CDASH, Controlled terminology and xml.
- Support the development of standards and drive their implementation within the organization.
- Clinical programming experience and experience working on a clinical
- Bachelor’s degree or higher and/or equivalent in computer science, data science/data engineering, mathematics, or another relevant scientific field (or equivalent theoretical/technical depth).
- Expert knowledge of SAS programming, Define.xml, SDTM aCRF, cSDRGs.
- Expert knowledge of data structures (e.g., CDISC SDTM, ADaM) and their implementation.
- Experience working in highly diverse teams within clinical research; cross-functional, global, multiregional.
- Project management skills.
- Highly organized with excellent written and verbal communication.
Benefits of Working in ICON:
Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.
At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.
ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.
#LI-Remote
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. Learn more about Our Culture at ICON
Day in the life
Similar jobs at ICON
Salary
Location
India, Chennai
Location
Bangalore
Chennai
Trivandrum
Bengaluru
Remote Working
Remote or Office
Business Area
ICON Strategic Solutions
Job Categories
Clinical Programming
Job Type
Permanent
Description
We are currently seeking a Senior Statistical Programmer and Principal Statistical Programmer to join our diverse and dynamic team. As a Senior /Princiapal Statistical Programmer at ICON, you will pla
Reference
JR142064
Expiry date
01/01/0001
Author
Swathy AnandanAuthor
Swathy AnandanSalary
Location
India, Bangalore
Location
Bangalore
Chennai
Trivandrum
Bengaluru
Remote Working
Hybrid
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Programming
Job Type
Permanent
Description
We are currently seeking a Clinical Data Science Programmer to join our diverse and dynamic team. As a Clinical Data Science Programmer at ICON, you will play an essential role in developing and imple
Reference
JR146195
Expiry date
01/01/0001
Author
Amrutha SaidalaAuthor
Amrutha SaidalaSalary
Location
US, Blue Bell (ICON)
Location
Blue Bell
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Programming
Job Type
Permanent
Description
We are currently seeking a Principal Statistical Programmer to join our diverse and dynamic team. As a Principal Statistical Programmer at ICON, you will be responsible for leading the design and impl
Reference
JR148092
Expiry date
01/01/0001
Author
Jamie PruittAuthor
Jamie PruittSalary
Location
Kenya
Location
Paris
Frankfurt
Budapest
Dublin
Milan
Warsaw
Johannesburg
Barcelona
Madrid
Lyon
Reading
Mechelen
Mannheim
Kenya
Assen
Swansea
Livingston
Remote Working
Remote or Office
Business Area
ICON Strategic Solutions
Job Categories
Clinical Programming
Job Type
Permanent
Description
We are seeking a highly skilled Senior Statistical Programmer with extensive experience in R Shiny application development and a strong background in clinical trial data standards. This role is ideal
Reference
JR138150
Expiry date
01/01/0001
Author
Jack FisherAuthor
Jack FisherSalary
Location
Japan, Tokyo
Location
Osaka
Tokyo
Remote Working
Remote or Office
Business Area
ICON Strategic Solutions
Job Categories
Clinical Programming
Job Type
Permanent
Description
We are currently seeking a Senior Statistical Programmer I to join our diverse and dynamic team. As a Senior Statistical Programmer I at ICON, you will play a crucial role in analyzing clinical trial
Reference
JR147211
Expiry date
01/01/0001
Author
Haruna YamabayashiAuthor
Haruna YamabayashiSalary
Location
Mexico, Mexico City
Location
Mexico City
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Programming
Job Type
Permanent
Description
We are currently seeking a Senior Statistical Programmer I to join our diverse and dynamic team. As a Senior Statistical Programmer I at ICON, you will play a crucial role in analyzing clinical trial
Reference
JR147918
Expiry date
01/01/0001
Author
Ana TelloAuthor
Ana Tello