Senior Statistician I
About the role
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“At ICON, it's our People
that set us Apart”
Are you passionate
about improving the quality of human life? If so, we invite you to join us
in creating a healthier world tomorrow.
ICON is a global
provider of outsourced development services to the pharmaceutical,
biotechnology and medical device industries. We specialize in the strategic
development, management and analysis of programs that support Clinical
Development - from compound selection to Phase I-IV clinical studies.
We started as a team
of 5 members in 1990 & today we are ranking at top 4 worldwide based on
revenue of 2015. Currently we have 12200+ employees across the globe. ICON
is a $1.575bn company having its presence across 89 offices in 37 countries.
Description
ICON is recruiting for Statisticians, Senior Statisticians. The successful
candidate will be responsible for statistical aspects
of clinical research projects. Providing statistical analysis
and interpretation of data and reporting of results.
Overview of the role
- Provides statistical support
for clinical studies, including study design, sample size
calculations, patient randomization, statistical analyses, interpretation
of data, and reporting of results.
- Writing statistical analysis plans, including the
definition of derived data sets, and the design of statistical tables,
figures, and data listings for clinical summary reports.
- Understands and uses relevant computer languages and
software packages (e.g. SAS)
- Monitors and verifies statistical analysis programs written
by statistical programmers.
- Conducts selected statistical analyses and interprets
results of these analyses.
Reviews and approves integrated clinical study reports. - Assists in the preparation of biostatistics input
to ICON research proposals.
Role Requirements
M.S. degree in statistics, biostatistics, or related field with a minimum of 4
years’ experience in the Pharmaceutical/ CRO industry,
Must be able to translate clients’ needs into statistical practice and educate
clients in the use of statistics.
Benefit Working with
ICON:
Other than working
with a great team of smart and energetic people, we also offer a very
competitive salary and benefits package that includes an excellent pension
scheme, private health care, and life assurance and staff recognition schemes.
This varies from country to country so a dedicated recruiter will discuss this
with you at interview stage.
PROCESS
Technical and
competency selection:
When you spot an
opportunity you’re interested in and submit an application, one of our Talent
Acquisition Specialists will contact you to evaluate your suitability for this
position, as well as for other openings within the business.
The evaluation will look
at your technical skills and your competencies – for example, delivering
excellence.
Interview
After this, we’ll let
you know if we’ll be progressing with your application. If you have been
successful at this stage, we will talk you through a telephone interview. This
will then be followed by an interview with our Hiring Manager, either
face to face or by tele-conference.
Offer
If you’re successful,
we will notify you with details of the offer, talk you through our culture and
values, answer any questions you may have – and above all, welcome you to the
ICON team.
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
12/10/2025
Summary
Zhong Yao's Journey at ICON Plc in China Zhong Yao's career in clinical research spans over two decades, with leadership roles across major CROs and a commitment to advancing healthcare in China.
Teaser label
IndustryContent type
BlogsPublish date
12/01/2025
Summary
How Data Moves Through a Clinical Trial Clinical research depends on one essential element: trustworthy data. Every safety decision, every statistical conclusion and every regulatory submission i
Teaser label
IndustryContent type
BlogsPublish date
11/28/2025
Summary
Quality and Compliance for New Entrants: A Plain Language Guide Quality and compliance can feel like dense subjects when you are entering clinical research for the first time. Many job
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