Biostatistician
- PREVENTION
- Nonprofits / องค์กรไม่แสวงหาผลกำไร
- 1726
- 19 Dec 2018
- 18 January 2019
Position Title: Biostatistician
Report to: Statistics and Data Management Manager
Organization:
PREVENTION, The Thai Red Cross AIDS Research Centre (TRCARC) in Bangkok, Thailand, is an organization under the umbrella of the Thai Red Cross Society. We provide outstanding HIV/AIDS treatment and care, foster innovative and responsible research, and train health care practitioners in HIV/AIDS.
Role Overview:
The Biostatistician is responsible for the design, analysis and reporting of medical research projects conducted by PREVENTION, the Thai Red Cross AIDS Research Centre (TRCARC).
Key Accountability/Responsibility
- Protocol development
- Assisting in the design of the study
- Performing appropriate sample size calculations
- Writing statistical analysis methods for the protocol
- Creating Statistical Analysis Plan (SAP)
- Author Statistical Analysis Plan
- Creating randomization list
- Creates randomization list
- Review of Case Report Forms (CRFs) and/or questionnaires
- Reviews content of the draft CRF and/or questionnaires against the protocol requirements and provide comments to ensure that data capture in those documents is relevant to all study endpoint and analyses
- Review of datasets
- Reviews the data tables received from data management team, checking that data is captured appropriately for any analyses
- Statistical analysis
- Program and validates statistical analyses
- Perform statistical analyses
- Report and/or manuscript writing
- Prepare and deliver reports for the analyses
- Prepare statistical methods sections for incorporation in abstracts, manuscripts
- Perform other tasks as assigned
Qualifications Specific
- Bachelor’s degree or Master degree in Biostatistics, Applied Statistics, or other related
- Minimum 3 years’ experience as a statistician in clinical trial or medical research
- Experience in team coordination
- Good writing and speaking in English language.
- Excellent conduct STATA software (others statistical software such as SAS, SPSS will be advantage)
- Regulatory requirements for clinical trials and medical research
- Ability to see the big picture, whilst still maintaining a focus on detail and implementation
Functional Competency
- Applied knowledge of advanced statistical models, such as generalized linear models, survival analyses and mixed models
- Data management skills for clinical trial and medical research
- Strong focus on quality and timely delivery of work
- Ability to work well and flexibly i.e. autonomously, in small teams and with a wide range of varying stakeholders
- Strong leadership and mentoring skills
- Excellent conduct STATA software (others statistical software such as SAS, SPSS will be advantage)