Senior Biostatistician II

"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.