Statistician/Statistical Programmer, Nairobi
- @TrendyJobbers | HR Outsourcing
- Full-time
- Posted 2 years ago
- Apply Before: May 12, 2024
- 0 Application(s)
- View(s) 538
Job Detail
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Job ID 1006029
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Career Level Officer
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Experience 5 Years
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Industry Development
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Qualifications Degree Bachelor
Job Description
Specific job responsibilities
- Contribute to the design of the study protocols including sample size estimation and power analysis.
- Perform random number generation and patient allocation for RCT.
- Develop Statistical Analysis Plans (SAP), TLF shell and dataset specifications for SDTM and ADaM.
- Be an SDTM and ADAM expert providing advice and training.
- Writing analysis programs to meet specifications of the SAP/lead statistical programming activities as trial programmer as well as making statistical programming decisions/recommendations at study/project level.
- Maintain proficiency in SAS and awareness of developments.
- Identify areas where new processes are required as well as create, review and update SOPs and Study Specific Procedures (SSPs).
- Analyzing and interpreting data from clinical trials and other studies.
- Liaise with the Senior Manager, Data Management and Biostatistics and coordinating office (Regional Operations Manager) to develop quarterly and yearly work-plans to determine activities and targets for the period.
- Identify and resolve data discrepancies in liaison with data managers.
- Participate in validation of Clinical Data Management Systems including edit check programs.
- Support study team in developing data collection tools and preparing data entry templates.
- Contribute to Case Report From (CRF) design and all other data management and statistical documentation.
- Perform additional management activities as required to provide timely and high-quality data for the purposes of analysis and/or regulatory submissions, database creation and testing.
- Maintain strict confidentiality of all privileged information regarding data and the organization.
- Assist in writing the statistical section of the CSR and ensure the CSR accurately describes the statistical methods and results of analyses.
- Ensure appropriate analysis procedures are used in statistical analyses.
- Create case report tabulations (CRT) from clinical trial data.
- Ability to work on multiple projects, plan, organize and prioritize activities.
- Be aware of up-and-coming changes to regulatory guidelines/requirements and awareness of emerging standards and associated impact to ongoing and future planned trials.
- Build and maintain effective working relationships with cross-functional teams.
- Comply with organization and industry standards (e.g. CDISC) and processes.
- Mentor other staff on statistical analysis/statistical programming.
Required skills
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