Thursday, 11 February 2021

Data Specialist at Kenya Medical Research – KEMRI

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: CGHR /177/02/21

Program description: The Kenya Medical Research Institute (KEMRI), Liverpool School of Tropical Medicine (LSTM) and the Centers for Disease Control and Prevention (CDC) will be conducting a large community-based study of Attractive Targeted Sugar Bait (ATSB) aimed at reducing malaria transmission in western Kenya. The 3-year project is part of a larger international ATSB consortium involving three countries in Africa, and international partners in the UK and USA. As part of this effort, KEMRI is searching for an exceptional trial manager with three years of relevant work experience to lead the study team

Reports to: Data Analyst

Essential Qualifications

  • Diploma in Computer Science, Information Technology, Mathematics or Statistics from a recognized institution
  • Excellent Microsoft Office skills
  • Experience working with relational database management systems

Desirable qualities

  • Experience in data cleaning and validation
  • Experience in source data verification other quality control activities
  • Attention to details and good work ethic
  • Good judgment in problem solving, awareness of own limitations and strong internal motivation
  • Ability to prioritize tasks and meet set deadlines
  • Must have good organizational skills
  • Flexible and able to work well with minimum supervision

Job Summary:

Reporting to the Data Analyst, the Data Specialist will be responsible for the data management procedures of the various sites within the study area. S/he will be expected to work on various databases and therefore should be able to prioritize tasks to meet set deadlines.

Duties and responsibilities

  • Conduct 100% source data verification, validation, and discrepancy management
  • Perform data cleaning and quality assurance and control
  • Ensure all missing data are captured in compliance to Good Clinical Practice (GCP) standards and within strict study timelines
  • Ensure that data is routinely backed up, anti-virus scans are conducted, and security measures are adhered to in order to protect data
  • Troubleshoot and solve common electronic data capture system problems
  • Ensure timely and accurate data entry and validation
  • Ensure timely response to data requests
  • Provide field support to the study teams, as needed
  • Perform any other duties as assigned by the immediate supervisor

Terms of Employment: 1(one) year contract as per KEMRI scheme of service and a Probation period for the first 3 months. Salary negotiable within the appropriate grade depending on education, experience and demonstrated competency.
Remuneration: Compensation is negotiable within the relevant grade, based on educational levels, relevant experience and demonstrated competency.

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