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Closing: Aug 16, 2022

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Published: Aug 5, 2022 (7 days ago)

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Job Summary

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Person Specifications

Education Requirements

  • Bachelor’s degree in clinical medicine and surgery or related field with a relevant Master’s degree is required.
  • Previous experience working as a researcher in a coordination role for at least 2 years will be an added advantage.
  • Knowledge and training in Good Clinical Practice and Human Subjects research is required.

Required experience and skills

  • Good interpersonal skills, organizational skills, strong service ethic, sensitivity to patients, professionalism, and attention to detail are required.
  • Demonstrable knowledge and extensive previous experience in clinical research is strongly preferred.
  • Proficient in MS Office application.
  • Experience in working
  • Paediatric experience is an added advantage.


Responsibilities

Person Specifications

Education Requirements

  • Bachelor’s degree in clinical medicine and surgery or related field with a relevant Master’s degree is required.
  • Previous experience working as a researcher in a coordination role for at least 2 years will be an added advantage.
  • Knowledge and training in Good Clinical Practice and Human Subjects research is required.

Required experience and skills

  • Good interpersonal skills, organizational skills, strong service ethic, sensitivity to patients, professionalism, and attention to detail are required.
  • Demonstrable knowledge and extensive previous experience in clinical research is strongly preferred.
  • Proficient in MS Office application.
  • Experience in working
  • Paediatric experience is an added advantage.


  • Assisting Principal investigators with implementation of study protocols, planning and problem-solving at IDI study site.
  • Assist the senior study coordinators in the setting-up and maintenance of regulatory approvals for the various protocols.
  • Contribute to the setting-up, maintaining and documenting regular communication within the study site.
  • Coordinate various aspects of the study including but not limited to; data collection, study log maintenance, data entry, biological specimen collection, storage and shipment at all study sites, including those located in Uganda.
  • Participate in various study procedures including consent, enrolment, biological specimen collection and follow-up of study participants
  • Participate in quality assurance and quality control of study data collected.
  • Supervise research nurses and study assistants and ensure that they achieve the objectives of the study as indicated in the protocol following the stipulated standard operating procedures.
  • Conduct ongoing performance reviews with direct reports as well as IDI-required performance appraisals.
  • Participate in the drafting of study progress and performance reports.
  • Participate in the development of materials and training of study staff to implement study procedures.
  • Participate in the procurement of study equipment and sundries
  • Participate in administration of study financial resources in accordance with IDI’s guidelines.
  • Contribute to the administration of study materials and resource inventory.
  • Contribute to the writing of scientific abstracts, papers or any other dissemination material from the study.
  • Attend relevant Research and Prevention Care and Treatment department meetings.


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