Prepare the statistical component of protocols which meet project objectives, health authority guidelines, and clinical trial methodology standards.
Develops and/or apply statistical theories, methods, and software programs such as SPSS, SAS, R
Provides specifications and directions to the clinicians/statistical
May partner in trial design and in establishing standards for clinical conduct, and the collection, management and/or reporting.
Present statistical results to non-statisticians

Qualifications

Bachelor’s degree in applied Statistics, Economics, Mathematics, Social Science or relevant fields from a reputable university.
Master’s degree in any of the aforementioned fields of study from a recognized institution
Qualifications in Research Methods, Statistics, Qualitative and Quantitative Research Methods
Proficient in SPSS, SAS, R or STATA
Experience in processing large data.
Experience in handling of protected patient health information
Experience in experimental design.
At least 3 years relevant work experience.