Job Title: Research Nurse (20 posts)
Reports to: Study Coordinator
Location: Mwanza, Simiyu, Geita and Pwani Regions
Job Summary
vacancy - Research Nurse, E-MOTIVE Programme
The E-MOTIVE research programme is seeking to deliver a reduction in morbidity and mortality from
postpartum haemorrhage (PPH). The E-MOTIVE research programme is seeking to hire the services of 20 Research Nurse/Midwives to be based within study regions (Mwanza, Simiyu, Geita and Pwani) under the Muhimbili University of Health and Allied Sciences. The Research Nurse/Midwife will ensure that the trial is run according to the protocol, Good Clinical Practice (GCP) and local regulatory requirements.
Main Duties:
Research:
• Ensure that the trial is conducted in accordance with the protocol and standard operating
procedures
• Assist clinicians and colleagues in setting-up patient pathways
• Attend trial-specific training and ensure that training is disseminated in the hospital allowing out of
hours adherence to the protocol
• Administer drugs and therapy according to the protocol
• Complete and maintain case report forms in accordance with trial requirements
• Ensure that all staff are aware of the correct treatment pathway for patients and time points for data
collection
• Ensure that data is captured in the source records and reported timely
• Be responsible for reporting adverse events in a timely manner at local level and escalate as
appropriate
• Collect information for regular reports on the progress of the trial
• Assist in site audits and monitoring visits carried out by regulatory authorities
• Assist with maintenance of accountability records, including retaining oversight of intervention
supply stock levels at site
• Participate in and contribute to study/country general activities e.g. meetings, training etc
Reports to: Study Coordinator
Location: Mwanza, Simiyu, Geita and Pwani Regions
Job Summary
vacancy - Research Nurse, E-MOTIVE Programme
The E-MOTIVE research programme is seeking to deliver a reduction in morbidity and mortality from
postpartum haemorrhage (PPH). The E-MOTIVE research programme is seeking to hire the services of 20 Research Nurse/Midwives to be based within study regions (Mwanza, Simiyu, Geita and Pwani) under the Muhimbili University of Health and Allied Sciences. The Research Nurse/Midwife will ensure that the trial is run according to the protocol, Good Clinical Practice (GCP) and local regulatory requirements.
Main Duties:
Research:
• Ensure that the trial is conducted in accordance with the protocol and standard operating
procedures
• Assist clinicians and colleagues in setting-up patient pathways
• Attend trial-specific training and ensure that training is disseminated in the hospital allowing out of
hours adherence to the protocol
• Administer drugs and therapy according to the protocol
• Complete and maintain case report forms in accordance with trial requirements
• Ensure that all staff are aware of the correct treatment pathway for patients and time points for data
collection
• Ensure that data is captured in the source records and reported timely
• Be responsible for reporting adverse events in a timely manner at local level and escalate as
appropriate
• Collect information for regular reports on the progress of the trial
• Assist in site audits and monitoring visits carried out by regulatory authorities
• Assist with maintenance of accountability records, including retaining oversight of intervention
supply stock levels at site
• Participate in and contribute to study/country general activities e.g. meetings, training etc
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Clinical:
• Practice always within relevant regulatory and ethics frameworks
• Comply with local institutions policies, procedures, standards and protocols, and collaborate with
other health care professionals to ensure these are observed
• Ensure that trials are undertaken in accordance with the terms approved by the local Ethics
Committee and other local regulatory bodies, if applicable
• Develop the role by using evidence-based practice and continuously improve own knowledge
• Provide ongoing advice and information to subjects
• Maintain patient confidentiality at all times
• Work autonomously to maximise recruitment into the trials
• Develop and maintain effective working relationships with all involved staff
Education and training:
Clinical:
• Practice always within relevant regulatory and ethics frameworks
• Comply with local institutions policies, procedures, standards and protocols, and collaborate with
other health care professionals to ensure these are observed
• Ensure that trials are undertaken in accordance with the terms approved by the local Ethics
Committee and other local regulatory bodies, if applicable
• Develop the role by using evidence-based practice and continuously improve own knowledge
• Provide ongoing advice and information to subjects
• Maintain patient confidentiality at all times
• Work autonomously to maximise recruitment into the trials
• Develop and maintain effective working relationships with all involved staff
Education and training:
• Consider the training and educational implications of the protocol and work with the Hub
management group to develop appropriate strategies to meet these in order to ensure the safe and
accurate implementation of the study by self and others (i.e. development of new standard operating
procedures and standards)
• Maintain an up to date knowledge of information procedures and to train other health care
professionals involved in patient management to work to the requirements of Good Clinical Practice
• Demonstrate a continuous process of professional and personal development in order to develop
own and others’ skills and to be aware of changes in professional practice
• Participation in training of trial team members (i.e. medical students, nurses/midwives)
Knowledge, Skills, Qualifications & Experience Required
Essential
• Educated to enrolled or registered Nurse/ Midwife level
• Knowledge and understanding of research governance regulations, principles and guidelines
including Good Clinical Practice, patient confidentiality, etc
• Excellent communication and listening skills with the ability to communicate effectively on many
levels (including via phone and email)
• Able to develop and acquire new skills as required
• Ability to delegate and work with others
• Very well organised, with good attention to detail
• Excellent time management skills with an ability to plan and prioritise
• Able to work independently, to prioritise their own workload to meet schedules and seek advice
when necessary
• Able to work across professional team and organizational boundaries
• Good IT skills and familiarity with MS Office applications
• A flexible, team-working attitude
• Excellent writing and communication skills
Recommended: JOIN US ON TELEGRAM FOR MORE THAN 2500 JOB POST AVAILABLE, CLICK HERE
management group to develop appropriate strategies to meet these in order to ensure the safe and
accurate implementation of the study by self and others (i.e. development of new standard operating
procedures and standards)
• Maintain an up to date knowledge of information procedures and to train other health care
professionals involved in patient management to work to the requirements of Good Clinical Practice
• Demonstrate a continuous process of professional and personal development in order to develop
own and others’ skills and to be aware of changes in professional practice
• Participation in training of trial team members (i.e. medical students, nurses/midwives)
Knowledge, Skills, Qualifications & Experience Required
Essential
• Educated to enrolled or registered Nurse/ Midwife level
• Knowledge and understanding of research governance regulations, principles and guidelines
including Good Clinical Practice, patient confidentiality, etc
• Excellent communication and listening skills with the ability to communicate effectively on many
levels (including via phone and email)
• Able to develop and acquire new skills as required
• Ability to delegate and work with others
• Very well organised, with good attention to detail
• Excellent time management skills with an ability to plan and prioritise
• Able to work independently, to prioritise their own workload to meet schedules and seek advice
when necessary
• Able to work across professional team and organizational boundaries
• Good IT skills and familiarity with MS Office applications
• A flexible, team-working attitude
• Excellent writing and communication skills
Recommended: JOIN US ON TELEGRAM FOR MORE THAN 2500 JOB POST AVAILABLE, CLICK HERE
Desirable:
• Experience in clinical trials
• Experience working with a donor funded project and/or with private sector
Application Guidelines:
Qualified and interested applicants are required to send electronic application letters and current CVs
describing their experience, qualification and three reference contacts by email.
Emails should be sent to fkaduma@gmail.com, mwampashi@gmail.com, beatricemwilike@yahoo.com not later than 3 September 2021.
Applicants should indicate in the email subject Research Nurse Position.
ONLY SHORTLISTED APPLICANTS WILL BE CONTACTED.
