women's cancer prevention research within the Clinical HIV Research Unit, a division of Wits Health Consortium Coordinator who will work to implement several clinical research projects within a women's health research research assistants, laboratory assistants, and clinic-based recruiters S/he will also oversee procurement areas: Oversee the day-to-day implementation of clinical research projects under the guidance of the relevant and clinic-based recruiters Oversee procurement and inventory management for the study clinic Prepare
women's cancer prevention research within the Clinical HIV Research Unit, a division of Wits Health Consortium Coordinator who will work to implement several clinical research projects within a women's health research research assistants, laboratory assistants, and clinic-based recruiters S/he will also oversee procurement areas: Oversee the day-to-day implementation of clinical research projects under the guidance of the relevant and clinic-based recruiters Oversee procurement and inventory management for the study clinic Prepare
women's cancer prevention research within the Clinical HIV Research Unit, a division of Wits Health Consortium Nurse who will assist in the implementation of clinical research projects within a women's health research screening, and enrolment S/he will assist with clinical procedures, scheduling of study visits, follow S/he will also assist with stock take in the study clinic Location: Helen Joseph Hospital – Johannesburg areas: Assist with the day-to-day implementation of clinical research projects under the guidance of the relevant
women's cancer prevention research within the Clinical HIV Research Unit, a division of Wits Health Consortium Nurse who will assist in the implementation of clinical research projects within a women's health research screening, and enrolment S/he will assist with clinical procedures, scheduling of study visits, follow S/he will also assist with stock take in the study clinic Location: Helen Joseph Hospital – Johannesburg areas: Assist with the day-to-day implementation of clinical research projects under the guidance of the relevant
epidemiological, clinical and basic science research and innovation It currently manages a number of clinical trials Plain and Khayelitsha Hospitals, and associated clinics Key performance areas: Conduct any pre-study entry evaluation for potential participants & offer clinical care to study participants Ensure that patients protocol without direct supervision Assist in all clinical aspects of the study, including venipuncture, point-of-care testing, drug administration and clinical observation when necessary Record accurately all
epidemiological, clinical and basic science research and innovation It currently manages a number of clinical trials Plain and Khayelitsha Hospitals, and associated clinics Key performance areas: Conduct any pre-study entry evaluation for potential participants & offer clinical care to study participants Ensure that patients protocol without direct supervision Assist in all clinical aspects of the study, including venipuncture, point-of-care testing, drug administration and clinical observation when necessary Record accurately all
COVID[1]19 protocols Work with the district manager, clinical mentor and other nurses to plan a tailored approach stakeholders in absence of district manager and clinical mentor Track changes made that lead to improved completion of clinical data on clinical form to ensure less than 5% of files have missing clinical information accurate daily, weekly and monthly reports to the Clinical mentor on work conducted Keep accurate records commodities and stock usage daily In the absence of the clinical mentor or when delegated to, complete the following
COVID[1]19 protocols Work with the district manager, clinical mentor and other nurses to plan a tailored approach stakeholders in absence of district manager and clinical mentor Track changes made that lead to improved completion of clinical data on clinical form to ensure less than 5% of files have missing clinical information accurate daily, weekly and monthly reports to the Clinical mentor on work conducted Keep accurate records commodities and stock usage daily In the absence of the clinical mentor or when delegated to, complete the following
participants, in line with study protocol, SOPs and Good Clinical Practice Conduct Informed Consent discussion according to study schedule Conduct data extraction from clinic registers, patient records or other relevant data of qualitative data if required Adhere to Good Clinical Practice Standards at all times Address relevant and personal abilities: Certification in good clinical practice (GCP) or NIH certification in the last be required Working within department of health clinics is required and working after hours may be required
participants, in line with study protocol, SOPs and Good Clinical Practice Conduct Informed Consent discussion according to study schedule Conduct data extraction from clinic registers, patient records or other relevant data of qualitative data if required Adhere to Good Clinical Practice Standards at all times Address relevant and personal abilities: Certification in good clinical practice (GCP) or NIH certification in the last be required Working within department of health clinics is required and working after hours may be required