Senior Biostatistician I

About the role

At ICON its 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 It culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability Delivery Collaboration Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touchpoint. In short to be the partner of choice in drug development.

Thats our vision. Were driven by it. And we need talented people who share it.

If youre as driven as we are join us. Youll be working in a dynamic and supportive environment with some of the brightest and the friendliest people in the sector and youll be helping shape an industry.

The Sr. Biostatistician l is responsible for planning monitoring organizing and reviewing activities of biostatisticians and programmers working on assigned studies of moderate complexity ensuring individual studies are delivered on time on budget to required quality.

The role

• Protocol input such as study design sample size calculations and patient randomization schemes
• Statistical aspects of case report form design
• Reviews study database structures edit checks and data management coding convention
• 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

What you need

• M.S. or Ph.D. degree in statistics biostatistics or related field.
• 4 years or more experience in a CRO or Pharmaceutical environment.
• Excellent verbal and written communication skills are required.
• Knowledge in applied parametric and nonparametric statistics and SAS programming skills.
• Should be able to translate clients needs into statistical practice and educate clients in the use of statistics.
• Experience working in oncology clinical trials is preferable but not essential.

Please use the below link for job application and quicker response.

Remote Work :

No