Workatele

Study Coordinator at Kenya Medical Research Institute – KEMRI, Nairobi, Kenya

Kenya Medical Research Institute – KEMRI

Study Coordinator at Kenya Medical Research Institute – KEMRI, Nairobi, Kenya

Kenya Medical Research Institute – KEMRI

Full time Job

Date Posted: June 17, 2024

Application deadline:

Expired on: June 3, 2024 5:00pm

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Job description

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.

Key Responsibilities:

  • Implementing clinical research projects and/or supervise designated aspects of the work
  • Establishing strategic partnerships for research, training, innovations, technology
  • Supervising junior professional and technical staff attached to his/her clinical research program,
  • Monitoring and evaluating implementation of research projects
  • Writing manuscripts, reports and translating research findings into lay language
  • Disseminating and translating research findings for evidence-based policy formulations and implementation
  • Develop and manage standard operating procedures (SOPs) for all study procedures
  • Plan and coordinate meetings for both internal project staff and external collaborators
  • Host/participate in scheduled conference calls with the international study partners.
  • Participate in development of research proposals in the relevant research thematic area Other Required Skills

Vacancy Requirements:

  • Medical degree from an accredited institution with a valid license to practice medicine in Kenya.
  • Prior experience conducting clinical research or participating in clinical trials.
  • Knowledge of STIs/HIV, including epidemiology, diagnosis, and treatment
  • Strong writing skills evidenced by peer review publications.
  • Familiarity with regulatory requirements and ethical guidelines governing clinical research (e.g., ICH-GCP, CITI)
  • Excellent interpersonal skills to deal effectively with clinicians, other study staff, participants, administrators, regulators, monitors, and sponsors.
  • Familiarity with the Microsoft Office Suite.
  • Excellent organizational skills to independently manage workflow.
  • Ability to prioritize quickly and appropriately
  • Ability to multi-task.
  • Meticulous attention to detail
  • Excellent written and verbal communication skills

Application deadline:

Expired on: June 3, 2024

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