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Holder of Advanced Diploma in Clinical Medicine from an accredited institution
Deputy Clinical Trial Manager
Posted: 15 Jun 2017 13:47
Deadline: 26 Jun 2017
Category: Health Professionals
Location: Africa , Tanzania , Mwanza
Employment: Full-Time
Education: Bachelor
Salary: Negotiable
About Company: The Mwanza Intervention Trials Unit (MITU) based at the National Institute for Medical Research (NIMR) campus in Mwanza, Tanzania is a collaborative research unit of the London School of Hygiene and Tropical Medicine and NIMR. The mission of MITU is to contribute to improving health through the development and evaluation of interventions against HIV and other health problems by conducting research, including clinical trials, to the highest international standards; to enhance the capacity to carry out such research in Tanzania and the East African region; and to contribute to the translation of research findings into health policy.
Phone: n.a
Contact name: hr
File: Download
• At least one year of experience working with school age children.
• Experience of working on vaccine-related research studies.
• Experience of working in East Africa.
• A postgraduate qualification in epidemiology or public health or equivalent
experience demonstrated through publications.
Assisting the Trial Manager with the day-to-day management of the clinical trial in Mwanza, Tanzania.
Consenting, screening and following up study participants.
Reporting and following up adverse events (AEs) and serious AEs.
Assisting the Trial Manager in dealing with clinical results and queries,
reviewing case report forms, and other relevant study documentation and
maintaining Study Master Files.
Assisting with communication between MITU/NIMR, the LondonSchool of
Hygiene & Tropical Medicine (LSHTM), the trial sponsor and the other trial
• Recruiting, coordinating, training and supervising field team staff in
MITU/NIMR (and other sites as required) in order to ensure that the trial is
conducted to GCP and other international trial standards.
• Participating in meetings and discussions to discuss research progress,
findings and any other aspects of the study.
• Assisting in submission of protocol amendments to ethics and regulatory
• Handling trial monitoring visits, including preparation of responses to
monitoring reports.
• Participating in writing up of the trial findings in reports and publications.
• Assisting with preparation of reports for the trial governance bodies (eg.
Clinical Steering Committee, Steering Committee, Data and Safety
Monitoring Board) and the funding agency .
• Travel to progress and coordination meetings as required.
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