General Summary
The senior Statistician shall be responsible for compiling and analyzing research/general clinic data at the IDI. He/she must be a diverse individual, showing broad technical, organizational, and communication skills, and be capable of working individually and in a team environment.

Key Responsibilities
• You will operate in a multi-disciplinary team comprising clinical and basic scientists with the support of senior statisticians and epidemiologists based at IDI and partner institutions worldwide.
• You will contribute to the design of trials and quality observational studies, support the development and deployment of statistical tools applicable to a broad range of clinical and laboratory-based research and conduct analyses of data.
• Advise and assist the research team on study design and data analysis
• Supervise and mentor junior Statisticians
• Perform independent statistical analyses on data generated by the project and assist in communicating the findings in peer-reviewed publications or reports.
• Carry out independent statistical analyses of clinical trials, under the supervision of the Head of Statistics unit; generate regular data safety monitoring committee reports and produce statistical reports.
• Advise and assist the research teams on study design and sample size in preparation of grant applications
• Manage the introduction and updating of Standard Operating Procedures for data processing and statistical matters as necessary.
• Contribute to the development of trial protocols, the design of the case report forms and databases in a multi-disciplinary environment.
• Contribute to the development of grant proposals
• Advise and support non-statistical researchers with regard to basic statistics and statistical analyses
• Follow STROBE and CONSORT statements for analyses of observational and clinical trial data respectively.

Person Specification
• The following is a list of desirable for efficient and effective job performance.
• It is not essential that the candidate must possess all of these.
• Relevant university education, with a minimum of a master’s degree in statistics or a related field.
• Ability to produce statistics for clinical management and research
• Ability to process, analyze, and present study results in a quality publishable format
• Experience in database design and data management
• Proficient in statistical analysis software eg. R, Python, STATA, etc.
• Experience in the development of Data Science models is an added advantage
• Should possess an updated certificate in Good Clinical Practice (GCP) and Human Subject Protection (HSP)