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The KEMRI Wellcome Trust Research Programme (KWTRP) is based within the KEMRI Centre for Geographic Medical Research - (Coast). Our core activities are funded by the Wellcome Trust. We conduct integrated epidemiological, social, laboratory and clinical research in parallel, with results feeding into local and international health policy. Our research platfor...
JOB PURPOSE:
This role is responsible for planning, developing, implementing and coordinating technical, operational and administrative aspects of the RVF003 clinical trial of a Rift Valley Fever vaccine and ensure compliance with the protocol, ethics and regulatory guidelines and in accordance with ICH GCP. To work closely with the PI, other internal and external stakeholders to ensure the trial is delivered within time, budget and scope. The post holder will need to be self-sufficient and be able to work with minimal supervision in a demanding environment, often with unpredictable timelines. The post is mentally demanding and extremely good communication is essential. The post holder may also be required to contribute to other associated projects.
Description:
REPORTS TO: Principal Investigator
DIRECTLY SUPERVISES: Study Coordinator
INDIRECTLY SUPERVISES: None.
BUDGET AND RESOURCE RESPONSIBILITY:
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JOB PURPOSE:
The post holder will be responsible for overseeing day-to-day clinical activities related to the RVF003 vaccine trial, evaluating the immunogenicity and safety of a Rift Valley Fever vaccine. Together with the Principal Investigator, the post holder will safeguard the health and welfare of the participants and ensure staff compliance with the protocol. Additionally, the post holder will perform and oversee clinical procedures and make trial-related medical decisions. He/she will work with the Principal Investigator to contribute to tasks preparatory to the project including protocol development and submissions, developing a study work plan, organising and conducting training for project-specific staff, and higher level responsibilities for ensuring field and laboratory procedures are carried out as well as data analysis, preparation of reports and manuscripts and correspondence with international collaborators and the sponsor. The post holder will need to be self-sufficient and be able to work with minimal supervision in a demanding environment, often with unpredictable timelines. The post is mentally demanding and extremely good communication is essential. The post holder may also be required to contribute to other associated projects.
Description:
REPORTS TO: Principal Investigator
DIRECTLY SUPERVISES: Clinical officers, fieldworkers, nurses
BUDGET AND RESOURCE RESPONSIBILITY: Management of study imprest
JOB DIMENSIONS:
KEY RESPONSIBILITIES:
QUALIFICATIONS:
DESIRABLE CRITERIA:
COMPETENCIES:
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