Principal Statistical Programmer
- Sofia, Dublin, Warsaw, Johannesburg, Reading
- ICON Full Service & Corporate Support
- Clinical Programming
Talent Acquisition Business Partner
- Full Service Division
About the role
This vacancy has now expired. Please click here to view live vacancies.
Principal Statistical Programmer
EMEA Remote
ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organizations.
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.
ICON’s Global Biostatistics & Statistical Programming team continues to grow and we are looking for experienced Programmers to join this diverse and growing group. Our team is currently over 600 employees in 30+ countries around the globe!
We have an exciting opportunity for a Principal Statistical Programmer to join ICON's Operational Centre of Excellence focusing on delivery and efficiency of programming services, which will leverage our expertise and best practices to produce top-quality output.
Overview of the Role:
The Principal Statistical Programmer will be responsible for creating, validating, and executing a range of statistical programs and applies extensive domain knowledge in the programming of datasets, tables, figures, and listings for quality and accuracy.
The Principal Statistical Programmer will lead and execute multiple projects in parallel, including ongoing coaching and mentorship of individual team members. In this client-facing role, you will be responsible for leading programming deliverables for complex assignments and building long-term relationships with clients in a partnership role.
Key responsibilities will include:
- Lead and manage the assigned programming team’s deliverables at the study and program level to ensure project objectives are met within budget, to agreed timelines and to the highest standard of quality.
- Proactively plan for and implement effective resource planning, task allocation and tracking of workload in accordance with agreed metrics (e.g. KPIs) and quality standards.
- Deliver high quality statistical programming deliverables for all assignments that consistently meets study timelines, quality standards, sponsor and/or contractual requirements.
- Efficient use of SAS, and adherence to SAS programming guidelines.
- Create and validate listing and safety outputs (analysis datasets, tables, figures)
- Create and validate efficacy outputs (analysis datasets, tables, figures)
- Create and validate complex programs (such as project or departmental macros)
- Create analysis dataset specifications (ADaM or client-specific)
- Set-up standard programming directories and start-up utilities.
- Create, document and validate project/study-macros at the table, listing and figure level.
- Liaise effectively with other ICON functions (e.g., PM, DM, MW), as required during the life of the project.
To be successful, you will need:
- 8+ years of experience successfully performing the role of Statistical Programmer, in the clinical research industry
- Experience with leading multiple projects in parallel – including Phase II and/or Phase III studies
- Experience leading oncology studies and knowledge of RECIST is strongly preferred
- Experience with creating and validating analysis datasets (CDISC ADaM standard), and Tables, Listings, and Figures
- Pinnacle 21 experience is strongly preferred
- Expert knowledge of SAS
- Professional leadership skills coupled with exceptional communication skills
- Education: Bachelor’s degree required (Statistics, Mathematics, Computer Science, or related scientific discipline); Master’s degree or PhD preferred
- EMEA based
Please note - we have roles available for Senior and Principal positions -
a decision on level of offer will be made after interview.
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 through the form below.
#LI-SA1, #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. See all locations Learn more about Our Culture at ICON
Day in the life
.jpg)
Teaser label
Inside ICONContent type
BlogsPublish date
01/17/2025
Summary
Five Reasons Why You Should Work at a Contract Research Organization Contract research organisations (CROs) play a pivotal role in advancing medical science, offering career opportunities that are
.jpg)
Teaser label
Career ProgressionContent type
BlogsPublish date
05/10/2024
Summary
Although many employers are returning to the office, we’re still seeing a mix of both video and in-person interviews in application processes. Early in 2020, the number of companies using video interv
.png)
Teaser label
Career ProgressionContent type
BlogsPublish date
12/21/2022
Summary
Salary expectations used to be something discussed after an interview process but now it’s something most recruiters typically ask within the first conversation. This is to ascertain if the remune
Similar jobs at ICON
Salary
Location
UK, Reading
Location
Budapest
Dublin
Warsaw
Lisbon
Bucharest
Johannesburg
Barcelona
Tallinn
Reading
Remote Working
Home or Office
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Programming
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
JR128125
Expiry date
01/01/0001
Author
Sophia CairnsAuthor
Sophia CairnsSalary
Location
UK, Reading
Location
Lisbon
Bucharest
Johannesburg
Barcelona
Bratislava
Tallinn
Reading
Gdansk
Remote Working
Home or Office
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Programming
Job Type
Permanent
Description
We are expanding our global Biostatistics and Programming team across Europe and are currently looking for experienced people to join this successful and evolving group, which forms part of our operat
Reference
JR130506
Expiry date
01/01/0001
Author
Sophia CairnsAuthor
Sophia CairnsSalary
Location
UK, Reading
Location
Reading
Remote Working
Home or Office
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Programming
Job Type
Permanent
Description
Principal Statistical Programmer ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research providing outsourced se
Reference
JR129190
Expiry date
01/01/0001
Author
Sophia CairnsAuthor
Sophia Cairns