Nursing Bursary Or Learnership To Study Bin 2015 Jobs in South Africa
Aj Personnel
- Last 7 days (4)
Research Nurse (enrolled Nurse X2 Fixed Term Contract For 12 Months)
Aj Personnel
Johannesburg
recruited participants in the different studies and assist other nurses in their daily work Location: Bara Chris Hani Baragwanath New Nurses Home, Soweto Key performance areas: To do study related duties as specified recognize respiratory illnesses in participants Compile study progress reports on number of participants enrolled relationship with clinic nurses/staff Follow-up participants who fail to attend their study visits Collect specimens consent forms Communicate routinely as needed to the study coordinator and Principal investigator regarding
share this job on whatsappResearch Nurse Pretoria, South Africa
Aj PersonnelPretoria
and other research-related duties in line with study protocols Location: Tshwane (Pretoria) Key performance performance areas: Inform participants about the study Screen potential participants and obtain informed informed consent according to SOPs Administer study questionnaires/interviews Draw blood/collect biological specimens Supervise the fieldwork team Develop and update study-specific job aides Collect participant data from and other study documents Safekeeping of project assets Facilitate training of staff on study protocol
Research Nurse Hillbrow, South Africa
Aj PersonnelHillbrow
performance areas: Inform participants about the study Screen potential participants and obtain informed informed consent according to SOPs Administer study questionnaires/interviews Draw blood/collect biological the fieldwork team if required Develop and update study-specific job aides Collect participant data from and other study documents Safekeeping of project assets Facilitate training of staff on study protocol timeously and accurately Provide regular updates on the study to key stakeholders Take ownership and accountability
Research Nurse Johannesburg, South Africa
Aj PersonnelJohannesburg
recruited participants in the different studies and assist other nurses in their daily work Location: Bara Chris Hani Baragwanath New Nurses Home, Soweto Key performance areas: To do study related duties as specified recognize respiratory illnesses in participants Compile study progress reports on number of participants enrolled relationship with clinic nurses/staff Follow-up participants who fail to attend their study visits Collect specimens consent forms Communicate routinely as needed to the study coordinator and Principal investigator regarding
Research Nurse (maternal And Obstetric Wits Rhi) From To (basic Plus Benefits) - Yearly
Aj PersonnelPretoria
and other research-related duties in line with study protocols Location: Tshwane (Pretoria) Key performance performance areas: Inform participants about the study Screen potential participants and obtain informed informed consent according to SOPs Administer study questionnaires/interviews Draw blood/collect biological specimens Supervise the fieldwork team Develop and update study-specific job aides Collect participant data from and other study documents Safekeeping of project assets Facilitate training of staff on study protocol
Research Nurses (x 2 Wits Rhi) From To (basic Plus Benefits) - Yearly
Aj PersonnelHillbrow
performance areas: Inform participants about the study Screen potential participants and obtain informed informed consent according to SOPs Administer study questionnaires/interviews Draw blood/collect biological the fieldwork team if required Develop and update study-specific job aides Collect participant data from and other study documents Safekeeping of project assets Facilitate training of staff on study protocol timeously and accurately Provide regular updates on the study to key stakeholders Take ownership and accountability
Clinical Trial Assistant Durban, South Africa
Aj PersonnelDurban
recruitment into the EFFECT study at different healthcare facilities Conduct any pre-study telephonic and/or in-person enrolment process and communicate with the study doctor and study nurse throughout the process Record all data explaining the study to patients and obtaining informed consent Assist with collecting study medication and and explaining to patients how to use the study medication, including completion of a medication diary participants' study information Ensure that accurate and complete records are kept with regard to study recruitment
Clinical Trial Assistant (12 Months Contract Mycology)
Aj PersonnelDurban
recruitment into the EFFECT study at different healthcare facilities Conduct any pre-study telephonic and/or in-person enrolment process and communicate with the study doctor and study nurse throughout the process Record all data explaining the study to patients and obtaining informed consent Assist with collecting study medication and and explaining to patients how to use the study medication, including completion of a medication diary participants' study information Ensure that accurate and complete records are kept with regard to study recruitment
Project Manager Hillbrow, South Africa
Aj PersonnelHillbrow
Description Main purpose of the job: The project manager/study coordinator is responsible for coordinating all activities according to good clinical practice, the study protocol, and the site's standard operating procedures protocol and GCP compliance Assist study team with efficient study start-up, conduct, and close-out Manage Manage regulatory updates throughout the study (New ICFs, Protocol Amendments, etc.) Proactively resolve investigators regarding participant welfare while on study Notify relevant parties of Serious Adverse Events
Project Managers (x 3 Wits Rhi) From To (basic Plus Benefits) - Yearly
Aj PersonnelHillbrow
Description Main purpose of the job: The project manager/study coordinator is responsible for coordinating all activities according to good clinical practice, the study protocol, and the site's standard operating procedures protocol and GCP compliance Assist study team with efficient study start-up, conduct, and close-out Manage Manage regulatory updates throughout the study (New ICFs, Protocol Amendments, etc.) Proactively resolve investigators regarding participant welfare while on study Notify relevant parties of Serious Adverse Events
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