Research Assistant, Kavi-Institute of Clinical Research Trial Manager, Kavi-Institute of Clinical Research

AD/5/73/23- 2 POSTS
BACKGROUND OF THE NATIONAL INSTITUTE OF HEALTH RESEARCH (NIHR), LONDON SCHOOL OF TROPICAL MEDICINE (LSTM) PROJECT

The NIHR Global Health unit on the prevention and management of stillbirths and Neonatal Deaths in Sub-Saharan Africa and South Asia, led from the Centre for Childbirth, Women’s and New-born Health at Liverpool School of Tropical Medicine United Kingdom (UK), is an established equitable multidisciplinary partnership between Africa, Asia and UK-based researchers. As an International Centre of Research excellence, our goal is to end preventable stillbirths and new-born deaths, ensure adequate support for parents and families whose baby dies and reduce associated stigma. Using a whole systems approach, we work across high burden settings in India, Kenya, Malawi, Pakistan, Tanzania, Uganda, Zambia and Zimbabwe.
We aim to develop, test and implement sustainable and cost-effective solutions to strengthen maternity and new-born care, reducing mortality and morbidity through high-quality, respectful and compassionate maternity and new-born care.

Purpose of the Position

The Research Assistant will offer postnatal support for parents, families and communities after stillbirth or neonatal death. This will include a range of activities such as gaining ethical approvals, recruitment and data collection, contributing to data analysis, data management, providing progress reports and liaising with stakeholders, Community Engagement and Involvement (CEI) groups and the wider team.

Duties and responsibilities

 To support the development, submission and approval of research protocols.
 To carry out recruitment of participants, collect, manage and contribute to analysis of data.
 To contribute to monitoring and evaluation activities.
 To assist in the co-ordination of local meetings
 To manage research and administrative activities in line with project activities.

Job requirements/Specifications:

Degree or Diploma in Nursing or related field
At least 3 years working experience in clinical trials preferably working with fistula patients and Lugina Africa Midwives Research Network (LAMRN)
Must have a valid GCP/ICH Training
Registered Midwife, Nurse or Allied Health professional will be added advantage
Experience, Knowledge and Competencies in the following areas: participatory research approaches, qualitative methods and analysis, working in maternity care (recent), Familiarity with data collection software; such as RedCap engagement with CEI groups, regional approaches to healthcare and publications and other dissemination activities
Terms of Appointment This a one (1) year full time contract renewable based on performance and by mutual consent.

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Use the emails(s) below to apply NOTESCLOSING DATE: FRIDAY, JUNE 14, 2023
 

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