Closing Date: 11th November 2018
Company Logo

Snaphunt Pte Ltd

We match jobs to talent for a skill and personality fit, across multiple specialist functions in Singapore.

Senior Statistician

Salary: 6000

  • 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: