Study Coordinator Job, Current Medical Jobs 2023,
Position: Study Coordinator (1 Position) K MR 6 Vacancy No. FN-11-02-2023
Reports to: Principal Investigator
Location: Kisumu
Duration: 1 Year Renewable Contract as per KEMRI Scheme of Service. The first 3 months is a probation period
Qualifications
- BSc Nursing, Clinical Medicine, Public Health or a related health research field.
- At least two year’s relevant experience managing and coordinating GCP compliant community or clinical trials.
- At least five years practical experience in the management of research teams.
- Experience in maintaining Study Master Files and other relevant study documents.
- Experience of preparing trial protocol amendments and submitting trial-related documents, including study reports, to ethics boards and/or regulatory authorities.
- Commitment to working as a member of a multidisciplinary and multicultural scientific team.
- Excellent inter-personal skills and a willingness to work with others to overcome problems as and when they arise.
- Excellent written and oral communication skills in English.
- Able to re-locate to Kisumu for this position.
- Willingness to work in urban and rural areas for study purposes.
Desirable qualities
- Prior work experience in research including implementation research studies.
- Communication skills in Swahili.
- Experience in drafting manuscripts for publication in peer-reviewed journals.
- Experience managing funds from international donor organisations
- Plan, manage and supervise the day-to-day management and study visits for ongoing trials.
- Prepare and submit trial documents to ethics and regulatory committees as required, including protocol amendments and six-monthly reports.
- Supervise responses to data queries, review case report forms and other relevant study documentation, and maintain Study Master Files.
- Participate in communication between KEMRI, study sponsors and the other study partners.
- Lead and supervise the study teams to ensure that the studies are conducted to GCP and international trial standards.
- Organise and participate in meetings regarding research progress, results and any other aspects of the studies.
- Organise procurements and orders for the studies and handle petty cash expenses for study activities.
- Assist in managing the project budgets and other project resources, liaise with administration staff in reviewing budgets, monitor expenditures and check financial reports.
- Coordinate study monitoring visits, including preparation of responses to monitoring
- Assist in drafting reports, publications and presentations of study results at national
- and international meetings and for trial governance bodies (eg,. The Data and Safety
- Monitoring Board)
- Provide weekly reports to the line manager and Principal Investigators on the study
- Travel to field sites as required to ensure the smooth running of study activities.
- Promote KEMRI Kargeno research and policy hub and its core values, and play a
- supportive role in the delivery of its day-to-day operations and strategic goals
- Undertake other duties, including support to other studies, as may be required by the
- trial Principal Investigators.
How to Apply
- All applicants must meet each selection criteria detailed in the minimum requirements.
- Must include a current CV with names of at least three referees.
- Must include copies of academic and professional certificates.
A duly signed application letter indicating the vacancy reference with copies of documents listed above should be sent to: hrrctp@kemri-rctp.org not later than February 28, 2023.
KEMRI IS AN EQUAL OPPORTUNITY EMPLOYER COMMITED TO DIVERSITY;PERSONS WITH DISABILITY, WOMEN, YOUTH AND THOSE FROM MARGINALIZED AREAS ARE ENCOURAGED TO APPLY.
Only short-listed candidates will be contacted
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Nancy Jepleting2023-02-14T15:15:43+03:00
https://jobcenterkenya.com/kemri-study-coordinator-job-sanofi-study/
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