participants in the different studies and assist other nurses in their daily work Location: Baragwanath NeoInspire performed Establish a working relationship with clinic nurses/staff Follow-up participants who fail to attend coordinator and Principal investigator regarding clinical management of subjects Attend and resolve queries education and training: Matric Qualified as an Enrolled Nurse Driver's License and able to drive Required minimum an Enrolled Nurse Professional body registration: Registered with the South African Nursing Council (SANC)
participants in the different studies and assist other nurses in their daily work Location: Baragwanath NeoInspire performed Establish a working relationship with clinic nurses/staff Follow-up participants who fail to attend coordinator and Principal investigator regarding clinical management of subjects Attend and resolve queries education and training: Matric Qualified as an Enrolled Nurse Driver's License and able to drive Required minimum an Enrolled Nurse Professional body registration: Registered with the South African Nursing Council (SANC)
epidemiological, clinical and basic science research and innovation It currently manages a number of clinical trials brings together leading academic researchers, clinical and public health leaders, non-governmental organisations Main purpose of the job: To join the sub-EFFECT clinical study site(s) team and manage day-to-day activities Rossmore NICD, Sandringham Key performance areas: Clinical study management Contribute to the development requirements Participate in regular meetings between the clinical teams and cover duties of the EFFECT trial study
epidemiological, clinical and basic science research and innovation It currently manages a number of clinical trials brings together leading academic researchers, clinical and public health leaders, non-governmental organisations Main purpose of the job: To join the sub-EFFECT clinical study site(s) team and manage day-to-day activities Rossmore NICD, Sandringham Key performance areas: Clinical study management Contribute to the development requirements Participate in regular meetings between the clinical teams and cover duties of the EFFECT trial study
responsible for coordinating all clinical trial activities according to good clinical practice, the study protocol performance areas: Oversee all operations in the clinical trial to ensure protocol and GCP compliance Assist queries and missing data with Investigators and Clinical Trials Assistants Communicate with CRO, Sponsor minimum work experience: 3-5 years experience in clinical trials/research Desirable additional education
responsible for coordinating all clinical trial activities according to good clinical practice, the study protocol performance areas: Oversee all operations in the clinical trial to ensure protocol and GCP compliance Assist queries and missing data with Investigators and Clinical Trials Assistants Communicate with CRO, Sponsor minimum work experience: 3-5 years experience in clinical trials/research Desirable additional education
design, implementation and continuous improvement of clinic- and community[1]based primary, HIV, and gender-affirming management, control and monitor expenditures of the clinic, adhering to relevant finance and procurement policies of the programme Support the implementation of clinical guidelines at a site level through on-site mentoring administrative procedures associated with accurate clinical record keeping and reporting including patient and accessibility of essential medicine for the clinic; and compliant and effective safety, quality control
design, implementation and continuous improvement of clinic- and community[1]based primary, HIV, and gender-affirming management, control and monitor expenditures of the clinic, adhering to relevant finance and procurement policies of the programme Support the implementation of clinical guidelines at a site level through on-site mentoring administrative procedures associated with accurate clinical record keeping and reporting including patient and accessibility of essential medicine for the clinic; and compliant and effective safety, quality control