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 accordance with SOPs Support data entry as needed Facilitate reimbursement for study participation, in collaboration and personal abilities: Certification in good clinical practice (GCP) or NIH certification in the last
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 accordance with SOPs Support data entry as needed Facilitate reimbursement for study participation, in collaboration and personal abilities: Certification in good clinical practice (GCP) or NIH certification in the last
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 Attend relevant internal and external meetings Facilitate reimbursement for study participation, in collaboration 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
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 accordance with SOPs Support data entry as needed Facilitate reimbursement for study participation, in collaboration and personal abilities: Certification in good clinical practice (GCP) or NIH certification in the last
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 Attend relevant internal and external meetings Facilitate reimbursement for study participation, in collaboration 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
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 accordance with SOPs Support data entry as needed Facilitate reimbursement for study participation, in collaboration and personal abilities: Certification in good clinical practice (GCP) or NIH certification in the last
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 accordance with SOPs Support data entry as needed Facilitate reimbursement for study participation, in collaboration and personal abilities: Certification in good clinical practice (GCP) or NIH certification in the last
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 Attend relevant internal and external meetings Facilitate reimbursement for study participation, in collaboration 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
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 accordance with SOPs Support data entry as needed Facilitate reimbursement for study participation, in collaboration and personal abilities: Certification in good clinical practice (GCP) or NIH certification in the last
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 Attend relevant internal and external meetings Facilitate reimbursement for study participation, in collaboration 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