participants from the community/Wits RHI study clinics into a study and conduct data collection and research study schedule
participants, in line with study protocol, SOPs and Good Clinical Practice
participants, in line with study protocol, SOPs and Good Clinical Practice
participants, in line with study protocol, SOPs and Good Clinical Practice
participants from the community/Wits RHI study clinics into a study and conduct data collection and research study schedule
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
participants from the community/Wits RHI study clinics into a study and conduct data collection and research to study schedule Support data extraction from clinic registers, patient records or other relevant data abreast with working trends by conducting weekly Clinic visits and assisting patients and caregivers Participate qualitative data collection Certification in good clinical practice (GCP) Empathetic with good communication the job: Working within the 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
participants from the community/Wits RHI study clinics into a study and conduct data collection and research to study schedule Support data extraction from clinic registers, patient records or other relevant data abreast with working trends by conducting weekly Clinic visits and assisting patients and caregivers Participate qualitative data collection Certification in good clinical practice (GCP) Empathetic with good communication the job: Working within the department of health clinics is required and working after hours may be required