Senior Statistician


| Singapore

Salary (USD) Not specified

Full Time | 0 Applicant(s)

Posted: 11 Oct 2018

About Company

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Job Description

Work with a leading employer in the FMCG industry

The Employer

Our client is a leading MNC within the FMCG industry that brings health through food to people globally. They have a regional headquarter in Singapore and are currently recruiting a Senior Statistician to join their Data Science team in their Research & Innovation hub in Singapore.

The Job

You will be a member of the Data Science Team and report to the Head of Data Science, R&I. This team is responsible for the biometrics expertise in assigned clinical studies within our Client's Early Life Nutrition business line. You will work in close collaboration with other Data Science team members including the Data Manager, Statistical Programmer and peer Statistician and work according to high scientific and operational standards.  

In this role you will provide state of-the-art statistical advice and support in the design, execution and interpretation of preclinical and clinical research . Your duties for this job would also include:

Advise on the methodological aspects and efficiency of clinical trial design

Provide statistical input to the clinical study protocol

Perform sample size calculations for a clinical study

Develop the Statistical Analysis Plan

Provide or check (complex) statistical analysis for study milestone deliverables

Review key clinical study documents, such as the clinical study report 

Provide statistical support for publications 

The Profile

To be able to achieve the above and be successful in this role you should ideally have: 

Master's degree (PhD would be a plus) in Statistics, Biostatistics or Mathematics with strong statistical content

In depth methodological expertise in medical statistics

Proficient programming expertise with SAS, R, EAST, Winbugs, Spotfire among others

Registration as Biostatistician or similar (CStat)

Extensive (at least 5 years) International clinical trial design expertise, including adaptive design, intervention, observational and real world evidence, with strong academic experience preferred

Knowledge of statistical principles, ICH-GCP guidelines and regulations

Demonstrated effective communications (written, verbal and presentation skills) in the internal multi-disciplinary project team and with external partners such as investigators, CROs 

Please apply for this role using the following link: