looking for an experienced Research Nurse who will assist in the implementation of clinical research projects informed consent, screening, and enrolment S/he will assist with clinical procedures, scheduling of study visits progress report for ongoing projects S/he will also assist with stock take in the study clinic Location: Helen Hospital – Johannesburg Key performance areas: Assist with the day-to-day implementation of clinical guidance of the relevant PIs and investigators Assist with all aspects of participant screening, informed
looking for an experienced Research Nurse who will assist in the implementation of clinical research projects informed consent, screening, and enrolment S/he will assist with clinical procedures, scheduling of study visits progress report for ongoing projects S/he will also assist with stock take in the study clinic Location: Helen Hospital – Johannesburg Key performance areas: Assist with the day-to-day implementation of clinical guidance of the relevant PIs and investigators Assist with all aspects of participant screening, informed
looking for an experienced Research Nurse who will assist in the implementation of clinical research projects consent, screening, and enrolment
Nurse to participate in a number of vital roles and assist in realizing the vision of the Division Main purpose advocate providing support and assistance as required and assistance as required Location: Cape Town: before commencement of any study related activities Assist with the follow-up of participants, including conducting Effect study protocol without direct supervision Assist in all clinical aspects of the study, including international standards of Good Clinical Practice (GCP) Assist in the preparation of study materials Participate
Nurse to participate in a number of vital roles and assist in realizing the vision of the Division Main purpose advocate providing support and assistance as required and assistance as required Location: Cape Town: before commencement of any study related activities Assist with the follow-up of participants, including conducting Effect study protocol without direct supervision Assist in all clinical aspects of the study, including international standards of Good Clinical Practice (GCP) Assist in the preparation of study materials Participate
facility in Westmead The overall scope of role is to assist the business with research and development of new
accordance with the protocol
accordance with the protocol Provide technical assistance (tool development and training) in HPV vaccination
accordance with the protocol Provide technical assistance (tool development and training) in HPV vaccination