Kenya Medical Research Institute (KEMRI) is a State Corporation established through the Science and Technology (Amendment) Act of 1979, which has since been amended to Science, Technology and Innovation Act 2013. The 1979 Act established KEMRI as a National body responsible for carrying out health research in Kenya.

Vacancy No. CRDR/07/09/23

Person specification:

•  Be a holder of a bachelor degree in Statistics, Biostatistics, Mathematics, Computer Science, or any related field from a recognized university.
•  Have at least three (3) year experience in data processing, management, and analysis in a health/medical research setting.
•  Have excellent working knowledge and experience with at least one statistical package for data manipulation and analysis (STATA, SPSS, SAS, R) and one database management software (SQL Server, MS Access).
•  Familiarity with modern database systems and information technologies including cloud server management.
•  Familiarity with EDCs such as REDCap, and ODK-based platforms such as ODK Survey, CommCare, SurvetCTO, etc
•  Be proficient in statistical and data management procedures, including data cleaning, manipulation, summaries, tables, listings, graphics, and inferential statistical output, as well as report generation.

Skills and Abilities:

•  Strong analytical ability, planning, and organizational skills.
•  Attention to detail
•  Ability to work with minimal supervision and within stipulated deadlines and schedules.
•  Excellent interpersonal and communication skills.
•  Be a team player and able to work in a multi-cultural environment.

Duties and Responsibilities:

•  Develop and maintain throughout life cycle of study projects, the Standard Operating Procedures (SOP), Data Management Plans (DMP), Data Quality Plans, and other plans as delegated/required, and ensure that these are followed according to study design/protocol and requirements.
•  Participate in study setup initiation, implementation, closure, and archiving procedures: i.e., CRF design, database design, database edit check’s, design/review, Data Management Plan review/approval and annotated CRF design.
•  Ensure Clinical database, external data files and analysis datasets are designed in a standard, accurate, complete, and consistent format conducive to analysis and possible regulatory submission.
•  Develop, review, and approve all SOPs, and job aids related to Data
• Management in collaboration with Quality Assurance and other departments as applicable.
•  Coordination of all data collection, cleaning and validation including, working with the trial monitors (where applicable) and resolving any data queries.
•  Maintain and update study laptops/tablets and other equipment used for data collection, ensuring data is downloaded daily/promptly and that forms are updated as needed.
•  Draft interim reports to the Principal Investigators, Sponsor, regulatory authorities, and oversight committees as requested by the Site Trial Manager.
•  Training users to use electronic data capture (EDC) systems. This includes creation of training documentation and running training sessions for end users.
•  Participate in planning meetings and scheduled conference calls with the study team and study partners/collaborators.
•  Ensure the conduct of the study is following the currently approved protocol/amendment(s), with current GCP guidelines and with applicable regulatory requirements.