Registered Mental Health Nurse developing strategic treatment plans to meet personalised needs. Communicates and builds rapport well to identify patient concerns and implement required support. Rigorous in risk assessment and emergency response for safe, attentive patient care.
Support follow-up of participants in accordance with protocol and SOPs
Provide individual and group counselling, testing and post-test counselling to potential participants in accordance with stated SOPs, and referring ineligible participants accordingly
Administer study product to participants as per study protocol procedures.
Set up examination rooms in accordance with protocol needs and conduct physical assessment to
participants to determine eligibility for study enrolment.
Identify and report to study clinicians any adverse events that are noticed and /or reported by study
participants.
Draw blood samples and other samples for screening and enrollment and follow up study procedures.
Ensures completion of source documentation and case report forms, checks for completion and accuracy,
and correct data errors when present.
Maintain confidentiality of study participants and adhere to principles of Human Subject Protection
(HSP) and Good Clinical Practice (GCP).
Assist with designated aspects of study including ensuring site compliance with study protocols, all
relevant procedures, policies, and regulations. Understand and adhere to study protocols, and other
appropriate regulations, procedures, and policies.
Review and reconcile data queries
Conduct quality control and assurance activities.
Write data quality assurance /study monitoring reports as needed follow-up of participants in accordance with protocol and SOPs.
Provide individual and group counselling, testing and post-test counselling to potential participants in accordance with stated SOPs, and referring ineligible participants accordingly
Administer study product to participants as per study protocol procedures.
Set up examination rooms in accordance with protocol needs and conduct physical assessment to
participants to determine eligibility for study enrolment.
Identify and report to study clinicians any adverse events that are noticed and /or reported by study
participants.
Draw blood samples and other samples for screening and enrollment and follow up study procedures.
Ensures completion of source documentation and case report forms, checks for completion and accuracy,
and correct data errors when present.
Maintain confidentiality of study participants and adhere to principles of Human Subject Protection
(HSP) and Good Clinical Practice (GCP).
Assist with designated aspects of study including ensuring site compliance with study protocols, all
relevant procedures, policies, and regulations. Understand and adhere to study protocols, and other
appropriate regulations, procedures, and policies.
Review and reconcile data queries
Conduct quality control and assurance activities.
Write data quality assurance /study monitoring reports as needed