about the company
A leading global developer of in-vitro diagnostics equipment and services is looking for a senior biostatistician
about the job
...
As a senior biostatistician, you will:
- Designs, analyzes, implements, and reports findings on targeted statistical research studies
- Works with investigators to formalize analysis plans and reporting specifications
- Assists in the preparation of clinical trial documents and reports, protocols, investigator brochures, scientific abstracts, peer-reviewed manuscripts, and responses to requests from regulatory agencies and other health authorities
- Reviews and analyzes safety reporting, biomarker analyses and other aspects of clinical trial monitoring.
- Plans and documents computer data file structure; develops, programs, manages, and maintains complex statistical databases; performs or supervises data entry.
about the manager/team
You will report to the research manager and work closely with other research personnel to ensure on-time delivery of projects.
skills and experience required
Masters or PhD degree in biostatistics, bioinformatics or related fields.
Minimum 3 years of experience in study design in a clinical trial settings.
Experience with oncology clinical trial will be advantageous.
Familiarity with SAS, R and other programming language will be a plus.
To apply online please use the 'apply' function, alternatively you may contact Allison Dong at +65 84173518.
(EA: 94C3609/R21100506)
show more
about the company
A leading global developer of in-vitro diagnostics equipment and services is looking for a senior biostatistician
about the job
As a senior biostatistician, you will:
- Designs, analyzes, implements, and reports findings on targeted statistical research studies
- Works with investigators to formalize analysis plans and reporting specifications
- Assists in the preparation of clinical trial documents and reports, protocols, investigator brochures, scientific abstracts, peer-reviewed manuscripts, and responses to requests from regulatory agencies and other health authorities
- Reviews and analyzes safety reporting, biomarker analyses and other aspects of clinical trial monitoring.
- Plans and documents computer data file structure; develops, programs, manages, and maintains complex statistical databases; performs or supervises data entry.
about the manager/team
You will report to the research manager and work closely with other research personnel to ensure on-time delivery of projects.
skills and experience required
Masters or PhD degree in biostatistics, bioinformatics or related fields.
...
Minimum 3 years of experience in study design in a clinical trial settings.
Experience with oncology clinical trial will be advantageous.
Familiarity with SAS, R and other programming language will be a plus.
To apply online please use the 'apply' function, alternatively you may contact Allison Dong at +65 84173518.
(EA: 94C3609/R21100506)
show more