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Associate Technical Research Officer / Moniteur d’Etude Clinique – Yaoundé

Elizabeth Glaser Pediatric AIDS Foundation

Yaoundé, Centre, Cameroon

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11 Apr. 2023

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Non spécifié

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Humanitaire

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Médecin humanitaire

Description
The Associate Technical Research Officer will be responsible for the preparation, implementation, and coordination of the UNITAID TB – Global – COVID-19 research project at the regional level. He/she will oversee each project’s research site in the assigned region and will supervise and support the Research Assistants/Study Nurses for the implementation of the study at the site level. He/she will report to each study Coordinator for project-related activities. For data and regulatory aspects of the research, he/she will report to the Data Manager and the in-country Principal Investigator. He/she will work under the direct supervision of the Study Coordinators.
  • Job title: Associate Technical Research Officer (Research Monitor)
  • Location:Yaounde, Centre Region
  • Number of Positions: 1
  • Primary Manager: Senior Research Technical Officer
Missions / Responsabilités / Activités
During the study preparation Phase:
  • Perform site preparation by identifying, and work with the procurement team to acquire and supply all materials needed to operationalize the research site.
  • Work closely with the Associate Regional Officers of the UNITAID TB – Global – COVID-19 Project to ensure local stakeholders (District Medical Officers, Hospital Director, and Community Structures) buy in of the study and needed support for implementation.
  • Assist the study coordinator in organizing onsite training for protocol and research procedures.
  • Ensure that all participating sites have data collection tools and study materials permanently in place.
  • Prepare with the study coordinators the site opening visits.

During The Study Enrolment Phase
  • Ensure that the enrolment takes place as planned in all study sites of the assigned region and provide appropriate support to the Research Assistant/Study Nurses.
  • Ensure the respect and the strict application of each study's Standards Operating Procedures (SOPs) at the site level.
  • Oversee the study enrolment at the site level and ensure the respect of the informed consent procedure.
  • Conduct regular monitoring visits according to the monitoring plan.
  • Assist data manager with data quality checks and ensure a response to data queries.
  • Monitor the progress of the study according to the protocol, SOPs, and the Good Clinical Practice (GCP) at the site level and report to the study coordinator.
  • Ensure the maintenance of the study Investigational Site File (ISF)
  • Ensure that the sensitive information (signed consent forms) is securely stored according to the protocol.
  • Ensure the completeness and regular update of the site investigator file.
  • Immediately report any serious adverse events to the study coordinator and the PI.
  • Supervise and mentor the site staff on all study-related issues.
Compétences / Exigences / Qualités
  • Medical Doctor with an MD degree or Senior registered graduate nurse
  • MPH degree in epidemiology, or public health, or Certificate in a research course will be appreciated.
  • Knowledge and comprehension of human subjects’ research, ethics, and of GCP.
  • Experience in clinical or operational research as a research assistant, data collector, site supervisor, or regional supervisor will be highly appreciated.
  • Experience in monitoring clinical and operational research data.
  • Excellent teamwork and coordination skills.
  • Excellent oral and written communication skills.
  • Perfect professional proficiency in English and French.
  • Availability to travel on the field on a regular basis
Profil du candidat
Documents de candidature
» Curriculum Vitae
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