Principal Statistician
About the role
This vacancy has now expired. Please click here to view live vacancies.
- The Biostatistics and Programming department is responsible for the statistical aspects of clinical trials including experimental design, statistical programming/analysis and reporting.
- This position manages the activities of Statisticians with an aim of meeting departmental goals.
- Manages the technical development of Statisticians and provides support and drives departmental initiatives
- The role also includes functioning at a senior technical level on projects as required.
- Management of the assigned line reports with regard to providing leadership for their effective development and high quality delivery of projects
- Provide support to senior management on the department budget management, project metrics and resourcing needs
- For Statisticial technical expertise, provide input into the following areas:
- Manage the statistical input to study design, analysis and reporting
- Collaboration with medical scientists in the design of clinical studies and the development of study protocols.
- Ensuring appropriate analysis procedures are used in statistical analyses
- Study reports accurately describe statistical methods and results of analyses
- Reviewing and approving statistical analysis plans, statistical analyses and study reports
- Provides input to ICON and client clinical and regulatory departments on statistical issues relating to client regulatory submissions. Responds to statistical questions raised by regulatory agencies and assists clients with statistical aspects of regulatory agency negotiations.
- Assist staff members with the identification of out of scope work and work with Contracts and Proposals to secure additional project funding
- Prepares and approves research proposals and budgets to provide statistical consulting and to conduct statistical analyses for clients in the pharmaceutical, biotechnology, computer, and manufacturing industries. As needed, participates in proposal defense meetings and makes presentations at marketing meetings with prospective clients.
- In conjunction with colleagues in other locations, as needed
- Organises and conducts regular departmental meetings
- Represents Biostatistics at interdepartmental meetings
- Maintenance of professional currency and a position of respect within the Pharmaceutical Industry including investigation of new software and attendance at appropropriate meetings and courses.
- Masters degree (or local equivalent) in biostatistics, statistics, or related field (required)
- Ph.D. degree (or local equivalent) in biostatistics, statistics, or related field (desirable).
- Significant proven and progressive experience pertaining to Biostatistics with prior relevant management experience. In depth proven experience should be in statistical applications in the pharmaceutical industry.
- Awareness of a broad range of Biostatistical techniques for example generalised linear models, nonparametric methods, analysis of binary/categorical data, survival data etc.
- Proficient SAS programming skills.
- Ability to critically review data.
- Strong skills in organizing, planning, problem solving.
- Excellent verbal and written communication skills.
- Good interpersonal skills and team player. Ability to interface with all levels both internally and externally.
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
Teaser label
Our PeopleContent type
BlogsPublish date
03/26/2026
Summary
Why Francis returned to ICON: building a long-term career in clinical research Francis Kayamba is a Clinical Research Associate based in Johannesburg, South Africa. He first joined ICON in February
Teaser label
Our PeopleContent type
BlogsPublish date
03/24/2026
Summary
Career paths are rarely straightforward, especially in the fast moving world of clinical research. For many professionals, gaining experience across organisations can provide valuable perspectiv
Teaser label
Our PeopleContent type
BlogsPublish date
03/16/2026
Summary
Driving Study Start-Up: James Pereira's Journey at ICON James Pereira's career in clinical research has been shaped by a single driving question: how do we get studies started faster? From his earl
Similar jobs at ICON
Salary
Location
Poland, Warsaw
Department
Full Service - Corporate Support
Location
Warsaw
Remote Working
Remote or Office
Business Area
ICON Full Service & Corporate Support
Job Categories
Drug Safety
Job Type
Permanent
Description
We are currently seeking a Senior Pharmacovigilance Associate to join our diverse and dynamic team. As a Senior Pharmacovigilance Associate at ICON, you will be instrumental in ensuring the safety and
Reference
JR148168
Expiry date
01/01/0001
Author
Magda KozuszekAuthor
Magda KozuszekSalary
Location
Poland, Warsaw
Location
Sofia
Prague
Budapest
Dublin
Riga
Warsaw
Lisbon
Bucharest
Belgrade
Barcelona
Madrid
Bratislava
Reading
Tbilisi
Remote Working
Remote or Office
Business Area
ICON Full Service & Corporate Support
Job Categories
Project Management
Job Type
Permanent
Description
About the roleAt ICON plc, we are committed to improving and saving lives through clinical research. As a Project Manager – Feasibility & Site Activation, you will play a critical role in driving the
Reference
JR148219
Expiry date
01/01/0001
Author
Magda KozuszekAuthor
Magda KozuszekSalary
Location
Argentina, Buenos Aires
Location
Buenos Aires
Remote Working
Hybrid
Business Area
ICON Full Service & Corporate Support
Job Categories
Study Start Up
Job Type
Permanent
Description
We are currently seeking a Site Specialist I (Study Start Up Associate I) to join our diverse and dynamic team. As a Site Specialist I at ICON, you will support investigator sites with key administrat
Reference
JR146306
Expiry date
01/01/0001
Author
Florencia PistolesiAuthor
Florencia PistolesiSalary
Location
Mexico, Mexico City
Location
Mexico City
Remote Working
Hybrid
Business Area
ICON Full Service & Corporate Support
Job Categories
Drug Safety
Job Type
Permanent
Description
We are currently seeking a Senior Pharmacovigilance Associate to join our diverse and dynamic team. As a Senior Pharmacovigilance Associate at ICON, you will be instrumental in ensuring the safety and
Reference
JR144856
Expiry date
01/01/0001
Author
Florencia PistolesiAuthor
Florencia PistolesiSalary
Location
Poland, Warsaw
Location
Sofia
Warsaw
Remote Working
Hybrid
Business Area
ICON Full Service & Corporate Support
Job Categories
Drug Safety
Job Type
Permanent
Description
We are currently seeking a Pharmacovigilance Assistant II to join our diverse and dynamic team. As a Pharmacovigilance Assistant II at ICON, you will play a critical role in ensuring the accurate coll
Reference
JR145206
Expiry date
01/01/0001
Author
Magda KozuszekAuthor
Magda KozuszekSalary
Location
US, San Antonio, TX, ICR
Location
San Antonio
Lawrence
Remote Working
Remote or Office
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Trial Liaison
Job Type
Permanent
Description
ICON’s field-based Clinical Trial Liaisons are highly trained site engagement specialists who support clinical trials by providing scientific and clinical support to investigators and site staff to en
Reference
JR145932
Expiry date
01/01/0001
Author
Muna NelkeAuthor
Muna Nelke