Senior Biostatistician II
TA Business Partner
About the role
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"At ICON, it's our People that set us Apart"
This is an exciting opportunity to work within a fast paced, busy
environment for a leading global provider of outsourced development services to
the pharmaceutical, biotechnology and medical device industries. ICON Clinical Research is Whole Owned Foreign
Company which founded in 1990 in
Ireland.
We expanded our business from 1995 in APAC region.
Currently we are hiring the Senior
Biostatistician II across APAC, preferably based in Seoul, Korea.
Role Summary
This
position will be accountable for the leadership of the Biostatistics and
Programming activities for high complexity studies, including
• Protocol input such as study design, sample
size calculations and patient randomization schemes
• Reviews study database structures, edit checks
and data management coding conventions
• Preparation of statistical analysis plans
including the definition of derived data, and the design of statistical tables,
figures, and data listings for clinical summary reports
• Statistical analyses
• Interpretation of data and reporting of results
• Writing of the statistical methods sections of
integrated study reports
and/or
accountable for the leadership of low complexity programs of studies. The
program of studies will typically lead to a regulatory submission.
The
position is accountable for planning, monitoring, organizing and reviewing
activities of biostatisticians and programmers working on the assigned study and/or
program of studies, ensuring individual studies and the program of studies are
delivered on time, on budget to required quality. Accountability also includes
maintenance of consistency across studies.
Experience and Qualification
• 8+ years of In depth proven relevant
experience in statistics, biostatistics or related field. In depth proven
experience must be in the pharmaceutical industry.
• In-depth knowledge of study designs, and
statistical analysis conventions in one or more therapeutic areas.
• Master’s degree or above in statistics
• Excellent verbal and written communication
skills both in Korean and English are required.
• Knowledge of clinical trials
methodology, regulatory requirements, statistics and statistical software
packages, including SAS are a must.
• Must be able to translate clients’ needs into
statistical practice and educate clients in the use of statistics.
• Good interpersonal and project management
skills.
Benefits of Working in ICON
Other
than working with a great team of smart and energetic people, we also offer a
very competitive benefits package. This
varies from country to country so a dedicated recruiter will discuss this with
you at interview stage.
We
care about our people as they are the key to our success. We provide an open
and friendly work environment where we empower people and provide them with
opportunities to develop their long term career.
What’s Next?
Following
your application you will be contacted by one of our dedicated recruiters and
if successful we will be able to provide you with more details about this
opportunity.
ICON
is an equal opportunity employer - M/F/D/V and committed to providing a
workplace free of any discrimination or harassment.
Application process
Once you find a job opening that fits your skills and interests, you can create an account, apply and check back on the progress of your application or apply for other roles. Once your application has been received, a confirmation email will be sent to your email.
Remember: this is our first time meeting you. Read the job description and highlight on your CV those experiences that we should learn about.
One of our experienced recruiters will read your profile and determine if you're fit for the role and the company. We are aware of instances where fake recruitment text messages and emails that can appear to come from ICON have been received by individuals. Always delete suspicious text messages or emails. Never give out personal financial information.
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